Day: November 9, 2021

SDS of cas: 123-11-5. Maitusong, J; Aimila, A; Zhang, JP; Mahinur, B; Maiwulanjiang, M; Aisa, HA in [Maitusong, Jumai; Aimila, Aoken; Zhang, Junping; Mahinur, Bakri; Maiwulanjiang, Maitinuer; Aisa, Haji Akber] Chinese Acad Sci, State Key Lab Basis Xinjiang Indigenous Med Plant, Xinjiang Tech Inst Phys & Chem, Urumqi 830011, Peoples R China; [Maitusong, Jumai; Aimila, Aoken; Zhang, Junping; Mahinur, Bakri; Maiwulanjiang, Maitinuer; Aisa, Haji Akber] Chinese Acad Sci, Key Lab Plant Resources & Chem Arid Zone, Xinjiang Tech Inst Phys & Chem, Urumqi 830011, Peoples R China; [Maitusong, Jumai; Aimila, Aoken] Univ Chinese Acad Sci, Beijing, Peoples R China; [Maitusong, Jumai] Coll Xinjiang Uyghur Med, Hotan, Peoples R China published Process optimization for the supercritical carbon dioxide extraction of Foeniculum vulgare Mill. seeds aromatic extract with respect to yield and trans-anethole contents using Box-Behnken design in 2021.0, Cited 30.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

Fennel (seeds of Foeniculum vulgare Mill.) is the widely used aromatic and medicinal plant throughout the world. In this research, supercritical carbon dioxide (SC-CO2) extraction was carried out to extract the aromatic extract from F vulgare seeds under various operating conditions, and aromatic extract samples were characterized for properties such as yield and trans-anethole content. A three-level Box-Behnken design from response surface method was applied to optimize the extraction parameters such as pressure, temperature, and extraction time with an aim to obtain high yield and rich trans-anethole content. The optimum extraction conditions were found to be 177 bar, 40 degrees C and 68 min where the predicted oil yield and trans-anethole contents were found to be 3.798% and 95 mg/g, respectively. Under the optimum conditions, the experimental oil yield was 3.85%, and the content of trans-anethole was 94 mg/g. The results were very close to the values predicted by the model. At the same time, the chemical compositions of the oils from two different extraction methods, hydrodistillation and SC-CO2, were compared. The chemical constituents of oils from two different extraction methods found to be the same, and they showed slight difference in terms of the quantity of the main chemicals. Antibacterial and antioxidant effects of the oils obtained by the two extraction methods were compared, and they showed similar effects.

Bye, fridends, I hope you can learn more about C8H8O2, If you have any questions, you can browse other blog as well. See you lster.. SDS of cas: 123-11-5

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Synthesis, structural, molecular docking and spectroscopic studies of (E)-N’-(4-methoxybenzylidene)-5-methyl-1H-pyrazole-3-carbohydrazide WOS:000595273300002 published article about CRYSTAL-STRUCTURE; AB-INITIO; BIOLOGICAL EVALUATION; DFT CALCULATIONS; SCHIFF-BASES; FORCE-FIELDS; FT-RAMAN; ANTIOXIDANT; IR; DERIVATIVES in [Karrouchi, Khalid; El Karbane, Miloud] Mohammed V Univ, Fac Med & Pharm, Lab Analyt Chem & Bromatol, Rabat, Morocco; [Brandan, Silvia A.] Univ Nacl Tucuman, Fac Bioquim Quim & Farm, Inst Quim Inorgan, Catedra Quim Gen, Ayacucho 471, RA-4000 San Miguel De Tucuman, Argentina; [Sert, Yusuf] Yozgat Bozok Univ, Sci & Art Fac, Sorgun Vocat Sch, Dept Phys, Yozgat, Turkey; [Radi, Smaail] Mohammed I Univ, Fac Sci, Dept Chem, Lab Appl Chem & Environm LCAE, Oujda 60000, Morocco; [Ferbinteanu, Marilena] Univ Bucharest, Fac Chem, Inorgan Chem Dept, Dumbrava Rosie 23, Bucharest 020462, Romania; [Garcia, Yann] Catholic Univ Louvain, Inst Condensed Matter & Nanosci, Mol Chem Mat & Catalysis IMCN MOST, Pl L Pasteur 1, B-1348 Louvain La Neuve, Belgium; [Ansar, M’hammed] Mohammed V Univ, Fac Med & Pharm, Lab Med Chem, Rabat, Morocco in 2021, Cited 73. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Product Details of 123-11-5

(E)-N’-4-methoxybenzylidene-5-methyl-1H-pyrazole-3-carbohydrazide (E-MBPC) has been synthesized and characterized by FT-IR, H-1 & C-13 NMR and ESI-MS spectroscopic methods. The (E)-configuration of hydrazonoic group was confirmed by single-crystal X-ray diffraction. Theoretical structures of E-MBPC in both gas phase and aqueous solution have been optimized by using hybrid B3LYP/6-311++G** calculations. Calculations in solution have shown that dipole moment increases from 7.97 D in the gas phase to 13.68 D in solution with solvation energy of -131.34 kJ/mol. Atomic charges have evidenced that the protonation of E-MBPC in solution could occur only in the N28 atom because those charges on this atom show negative values. Mapped MEP surfaces show that the nucleophilic sites is located on the O21 and N28 atoms including the N16 atom while the electrophilic sites are observed on the N24-H27 and N18-H19 bonds. NBO calculations support the high stability of E-MBPC in solution while frontier orbitals studies suggest low reactivity of E-MBPC in both media, as compared with the (E)-N’-(4-(dimethylamino)benzylidene)-5-methyl-1H-pyrazole-3-carbohydrazide derivative. The vibrational assignments of 93 vibration modes expected for E-MBPC were reported together with the corresponding force fields and force constants in both media. The predicted Raman and Ultraviolet-visible spectra were also reported for E-MBPC at the same level of theory. Good correlations were obtained between the predicted H-1- and C-13 NMR spectra and the corresponding experimental ones. In addition, molecular docking studies between the title ligand and 4AMJ protein were performed. Docking results revealed that the title compound can be designed as a potential anti-diabetic agent. (C) 2020 Elsevier B.V. All rights reserved.

Welcome to talk about 123-11-5, If you have any questions, you can contact Karrouchi, K; Brandan, SA; Sert, Y; El Karbane, M; Radi, S; Ferbinteanu, M; Garcia, Y; Ansar, M or send Email.. Product Details of 123-11-5

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Design, synthesis and biological evaluation of new 1,3-thiazole derivatives as potential anti-inflammatory agents WOS:000663587400007 published article about DISCOVERY; THIAZOLE in [Modric, Marina] Fidelta Ltd, Chem, Prilaz Baruna Filipovica 20, HR-10000 Zagreb, Croatia; [Bozicevic, Marin; Skoric, Irena] Univ Zagreb, Fac Chem Engn & Technol, Dept Organ Chem, Marulicev Trg 19, HR-10000 Zagreb, Croatia; [Faraho, Ivan; Bosnar, Martina] Fidelta Ltd, Pharmacol Vitro, Prilaz Baruna Filipovica 29, HR-10000 Zagreb, Croatia in 2021, Cited 18. COA of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Thiazoles are widely recognized as nuclei of great value for obtaining molecules with various biological activities, including analgesic, anti-inflammatory, anti-HIV, antidiabetic, antitumor and antimicrobial. A library of 26 thiazole derivatives as fragments were designed, synthesized and evaluated for their anti-inflammatory activities. Some screened compounds showed promising results and were found to be potent in the series by inhibiting LPS-induced TNF alpha and IL-8 release with IC50 values in mu M range without cytotoxic activity. (C) 2021 Elsevier B.V. All rights reserved.

COA of Formula: C8H8O2. Welcome to talk about 123-11-5, If you have any questions, you can contact Modric, M; Bozicevic, M; Faraho, I; Bosnar, M; Skoric, I or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Characterization of key aroma compounds in Chinese rice wine using gas chromatography-mass spectrometry and gas chromatography-olfactometry WOS:000469331900002 published article about ODOR-ACTIVE COMPOUNDS; VOLATILE COMPOUNDS; LIQUORS; FERMENTATION; YEAST; QU in [Yu, Haiyan; Xie, Tong; Xie, Jingru; Tian, Huaixiang] Shanghai Inst Technol, Dept Food Sci & Technol, 100 Haiquan Rd, Shanghai 201418, Peoples R China; [Ai, Lianzhong] Univ Shanghai Sci & Technol, Sch Med Instrument & Food Engn, Shanghai 200093, Peoples R China in 2019.0, Cited 28.0. Quality Control of Benzyl Alcohol. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

To determine the key aroma compounds in Chinese rice wine (CRW), four types of CRW (YH, JF, SN, and XX) were analyzed by gas chromatography-mass spectrometry (GC-MS), gas chromatography-olfactometry (GC-O), and sensory evaluation. The contributions of the key aroma compounds to the flavor characteristics were determined by partial least squares regression. Sixty-one aroma compounds were detected. Twenty-five components were identified as odor-active compounds. On the basis of their odor active values, 18 odor-active compounds were determined as key aroma compounds. Ethyl isovalerate, ethyl butyrate, ethyl acetate, ethyl hexanoate, and phenylethyl alcohol were key aroma compounds in all four types of wine. The unique key aroma compounds of JF wine were isovaleraldehyde and isoamyl acetate; those of XX wine were 1-butanol, benzaldehyde, ethyl benzoate, ethyl phenylacetate, 2-octanone, and furfural; that of YH wine was ethyl 2-methylbutyrate; and those of SN wine were 1-butanol, 1-hexanol, 2-butenoic acid ethyl ester, and 3-methyl-1-butanol.

Quality Control of Benzyl Alcohol. Welcome to talk about 100-51-6, If you have any questions, you can contact Yu, HY; Xie, T; Xie, JR; Ai, LZ; Tian, HX or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Structure-Activity Relationship for the Oxadiazole Class of Antibacterials WOS:000526401400022 published article about PLASMA-PROTEIN BINDING; UPDATE; DRUGS in [Boudreau, Marc A.; Ding, Derong; Meisel, Jayda E.; Janardhanan, Jeshina; Spink, Edward; Peng, Zhihong; Qian, Yuanyuan; Yamaguchi, Takao; Testero, Sebastian A.; O’Daniel, Peter I.; Leemans, Erika; Lastochkin, Elena; Song, Wei; Mobashery, Shahriar; Chang, Mayland] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA; [Schroeder, Valerie A.; Wolter, William R.; Suckow, Mark A.] Univ Notre Dame, Freimann Life Sci Ctr, Notre Dame, IN 46556 USA; [Schroeder, Valerie A.; Wolter, William R.; Suckow, Mark A.] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA in 2020.0, Cited 12.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Product Details of 99-93-4

A structure-activity relationship (SAR) for the oxadiazole class of antibacterials was evaluated by syntheses of 72 analogs and determination of the minimal-inhibitory concentrations (MICs) against the ESKAPE panel of bacteria. Selected compounds were further evaluated for in vitro toxicity, plasma protein binding, pharmacokinetics (PK), and a mouse model of methicillin-resistant Staphylococcus aureus (MRSA) infection. Oxadiazole 72c shows potent in vitro antibacterial activity, exhibits low clearance, a high volume of distribution, and 41% oral bioavailability, and shows efficacy in mouse models of MRSA infection.

Welcome to talk about 99-93-4, If you have any questions, you can contact Boudreau, MA; Ding, DR; Meisel, JE; Janardhanan, J; Spink, E; Peng, ZH; Qian, YY; Yamaguchi, T; Testero, SA; O’Daniel, PI; Leemans, E; Lastochkin, E; Song, W; Schroeder, VA; Wolter, WR; Suckow, MA; Mobashery, S; Chang, M or send Email.. Product Details of 99-93-4

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

HPLC of Formula: C5H8O2. Authors Korff, M; Imberg, L; Will, JM; Buckreiss, N; Kalinina, SA; Wenzel, BM; Kastner, GA; Daniliuc, CG; Barth, M; Ovsepyan, RA; Butov, KR; Humpf, HU; Lehr, M; Panteleev, MA; Poso, A; Karst, U; Steinmetzer, T; Bendas, G; Kalinin, DV in AMER CHEMICAL SOC published article about in [Korff, Marvin; Imberg, Lukas; Kastner, Gregor A.; Barth, Maximilian; Lehr, Matthias; Kalinin, Dmitrii, V] Univ Munster, Inst Pharmaceut & Med Chem, D-48149 Munster, Germany; [Will, Jonas M.; Karst, Uwe] Univ Munster, Inst Inorgan & Analyt Chem, D-48149 Munster, Germany; [Bueckreiss, Nico; Bendas, Gerd] Univ Bonn, Pharmaceut Inst, D-53121 Bonn, Germany; [Kalinina, Svetlana A.; Humpf, Hans-Ulrich] Univ Munster, Inst Food Chem, D-48149 Munster, Germany; [Wenzel, Benjamin M.; Steinmetzer, Torsten] Philipps Univ Marburg, Inst Pharmaceut Chem, Dept Pharm, D-35032 Marburg, Germany; [Daniliuc, Constantin G.] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany; [Ovsepyan, Ruzanna A.; Butov, Kirill R.; Panteleev, Mikhail A.] Dmitriy Rogachev Natl Med Res Ctr Pediat Hematol, Lab Translat Med, Moscow 117997, Russia; [Ovsepyan, Ruzanna A.; Butov, Kirill R.; Panteleev, Mikhail A.] Russian Acad Sci, Ctr Theoret Problems Physicochem Pharmacol, Moscow 119991, Russia; [Panteleev, Mikhail A.] Lomonosov Moscow State Univ, Fac Phys, Moscow 119991, Russia; [Panteleev, Mikhail A.] Moscow Inst Phys & Technol, Fac Biol & Med Phys, Dolgoprudnyi 141700, Russia; [Poso, Antti] Univ Eastern Finland, Fac Hlth Sci, Sch Pharm, Kuopio 70211, Finland; [Poso, Antti] Univ Hosp Tubingen, Dept Internal Med 8, D-72076 Tubingen, Germany in 2020, Cited 75. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1

We herein report the conventional and microscale parallel synthesis of selective inhibitors of human blood coagulation factor XIIa and thrombin exhibiting a 1,2,4-triazol-5-amine scaffold. Structural variations of this scaffold allowed identifying derivative 21i, a potent 29 nM inhibitor of FXIIa, with improved selectivity over other tested serine proteases and also finding compound 21m with 27 nM inhibitory activity toward thrombin. For the first time, acylated 1,2,4-triazol-5-amines were proved to have anticoagulant properties and the ability to affect thrombin- and cancer-cell-induced platelet aggregation. Performed mass spectrometric analysis and molecular modeling allowed us to discover previously unknown interactions between the synthesized inhibitors and the active site of FXIIa, which uncovered the mechanistic details of FXIIa inhibition. Synthesized compounds represent a promising starting point for the development of novel antithrombotic drugs or chemical tools for studying the role of FXIIa and thrombin in physiological and pathological processes.

HPLC of Formula: C5H8O2. Welcome to talk about 80-59-1, If you have any questions, you can contact Korff, M; Imberg, L; Will, JM; Buckreiss, N; Kalinina, SA; Wenzel, BM; Kastner, GA; Daniliuc, CG; Barth, M; Ovsepyan, RA; Butov, KR; Humpf, HU; Lehr, M; Panteleev, MA; Poso, A; Karst, U; Steinmetzer, T; Bendas, G; Kalinin, DV or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Synthesis and characterization of nanocrystalline hydroxyapatite and its catalytic behavior towards synthesis of 3,4-disubstituted isoxazole-5(4H)-ones in water WOS:000478695000001 published article about ONE-POT SYNTHESIS; SOLVENT-FREE SYNTHESIS; 3-COMPONENT SYNTHESIS; RECYCLABLE CATALYST; GREEN SYNTHESIS; PALLADIUM NANOPARTICLES; HETEROGENEOUS CATALYST; EFFICIENT SYNTHESIS; COUPLING REACTIONS; GRAPHENE OXIDE in [Maleki, Behrooz; Chahkandi, Mohammad; Tayebee, Reza; Kahrobaei, Sepideh] Hakim Sabzevari Univ, Dept Chem, Sabzevar 9617976487, Iran; [Alinezhad, Heshmatollah] Univ Mazandaran, Fac Chem, POB 47416-95447, Babol Sar, Iran; [Hemmati, Saba] Payame Noor Univ, Dept Chem, Tehran, Iran in 2019.0, Cited 70.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Application In Synthesis of 3-Hydroxybenzaldehyde

In the present work, the nanocrystalline particles of hydroxyapatite (HAp) using an easy alkoxide-based sol-gel technique including triethyl phosphate [PO (OC2H5)(3)] and Ca (NO3)(2)center dot 4H(2)O as P and Ca precursors have been synthesized. The sample characterization was performed by X-ray diffraction, Fourier transform-infrared analysis, scanning electron microscopy, thermal analysis (thermogravimetric analysis/differential thermal analysis), and elemental analysis of energy-dispersive X-ray analysis. It is interesting that single phase of HAp was obtained at a low firing temperature of 500 degrees C. Modified Scherrer equation as the Williamson-Hall method was applied for the measurement of crystallite size distributions and micro-strain of the sample. The determined crystallite size by complementary technique of transmission electron microscopy has good consistency with those obtained from the Scherrer formula. Moreover, we reported the one-pot synthesis of 3,4-disubstituted isoxazole-5(4H)-ones through the aqueous solution reaction of three components of ethyl acetoacetate, hydroxylamine hydrochloride and various aromatic aldehydes at room temperature. This protocol offers several advantages, including a simple work-up procedure, very short reaction times (under 25 min), in accordance with the principles of green chemistry, recyclability, excellent yields (87-98%) and environmentally friendly.

Application In Synthesis of 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Maleki, B; Chahkandi, M; Tayebee, R; Kahrobaei, S; Alinezhad, H; Hemmati, S or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Formula: C7H6O2. I found the field of Chemistry very interesting. Saw the article Metal Free Sulfonic Acid Functionalized Carbon Catalyst for Green and Mechanochemical Synthesis of Perimidines published in 2020.0, Reprint Addresses Agarwal, S (corresponding author), MLSU, Dept Chem, Synthet Organ Chem Lab, Udaipur 313001, Raj, India.. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde.

A new and scalable mechanochemical approach has been developed for the synthesis of perimidine derivatives using an efficient and recyclable catalyst, carbon sulfonic acid under metal-free conditions. A wide variety of aldehydes displayed cyclo-condensation reaction with 1,8-diaminonaphthalene in EtOH under ambient reaction conditions via grind-stone technique to produce substituted perimidines in excellent yields (95-99 %) in a very short reaction time. This method has interesting features like single-step synthesis, high functional group tolerance, transition-metal free synthesis, high atom-economy, recyclable catalyst, no need of tedious purification process, gram-scale synthesis, high green chemistry matrix (Eco-score and E-factor) that make this protocol green and eco-friendly.

About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Sahiba, N; Sethiya, A; Soni, J; Agarwal, S or concate me.. Formula: C7H6O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2020 ORG LETT published article about CARBOXYLIC-ACIDS; BOND FORMATION; ACTIVATION; ANNULATION; AMINATION; ALKYNES; FUNCTIONALIZATION; ALKENYLATION; SELECTIVITY; ARYLATION in [Gao, Yang; Nie, Jianhong; Li, Xianwei; Chen, Qian; Huo, Yanping] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China; [Hu, Xiao-Qiang] South Cent Univ Nationalities, Sch Chem & Mat Sci, Key Lab Catalysis & Energy Mat Chem, Minist Educ, Wuhan 430074, Hubei, Peoples R China; [Hu, Xiao-Qiang] South Cent Univ Nationalities, Sch Chem & Mat Sci, Hubei Key Lab Catalysis & Mat Sci, Wuhan 430074, Hubei, Peoples R China; [Li, Yibiao] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529090, Guangdong, Peoples R China in 2020, Cited 53. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1. Safety of (E)-2-Methylbut-2-enoic acid

A method for the synthesis of diverse polysubstituted quinolines from readily available acrylic acids and anthranils has been developed. The weakly coordinating -COOH directing group, which can be tracelessly removed in the cascade cyclization, is essential for this reaction. Diverse polysubstituted quinolines were obtained under mild reaction conditions with simple H2O and CO2 as byproducts. More importantly, 1,2,3,4-tetrahydroacridine, which is the core skeleton of tacrine (an Alzheimer’s disease drug), was conveniently synthesized.

Safety of (E)-2-Methylbut-2-enoic acid. Welcome to talk about 80-59-1, If you have any questions, you can contact Gao, Y; Nie, JH; Li, YB; Li, XW; Chen, Q; Huo, YP; Hu, XQ or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 120-14-9. Authors Ma, S; Cui, JW; Rao, CH; Jia, MZ; Chen, YR; Zhang, J in ROYAL SOC CHEMISTRY published article about in [Ma, Shuai; Cui, Jing-Wang; Rao, Cai-Hui; Jia, Meng-Ze; Chen, Yun-Rui; Zhang, Jie] Beijing Inst Technol, Sch Chem & Chem Engn, MOE Key Lab Cluster Sci, Beijing Key Lab Photoelect Electrophoton Convers, Beijing 102488, Peoples R China in 2021.0, Cited 48.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9

An eco-friendly and economical approach for the photocatalytic oxidation of organic inter-mediates by air under mild conditions is highly desirable in green and sustainable chemistry, where the photogeneration of active oxygen species plays a key role in improving conversion efficiency and selectivity. By using pyridinium derivatives as molecular mediators for electron transfer and energy transfer, the simultaneous activation of O-2 from air into superoxide radicals and singlet oxygen species can be achieved, and a photoinduced electron transfer catalytic system for the oxidation of alcohols has been developed. Thus, we have successfully simplified the complicated catalytic system into a single molecular catalyst without any additional noble metals and co-catalysts/additives. The current photocatalytic system shows high catalytic efficiency not only for aromatic alcohols but also for aliphatic alcohols that are generally difficult to undergo aerobic oxidation at room temperature under air atmosphere, representing an ideal photocatalytic platform for green and economical organic syntheses.

Welcome to talk about 120-14-9, If you have any questions, you can contact Ma, S; Cui, JW; Rao, CH; Jia, MZ; Chen, YR; Zhang, J or send Email.. Product Details of 120-14-9

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles