Category: 123-11-5

Product Details of 123-11-5. Authors Rabon, AM; Doremus, JG; Young, MC in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Rabon, Allison M.; Doremus, Jared G.; Young, Michael C.] Univ Toledo, Sch Green Chem & Engn, Dept Chem & Biochem, Toledo, OH 43606 USA in 2021.0, Cited 42.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Metal-organic frameworks (MOFs) show promise for catalysis applications due to their porosity, high internal surface area, and structural adaptability. Typical acetylation reactions of aldehydes require elevated temperatures and excess alcohol to drive the reactions to completion. In this current work, MOF-808 is used as a heterogeneous catalyst for acetylation of aldehydes in methanol using a mild photothermal process. Optimized conditions gave 72% yield of 2-(dimethoxymethyl)naphthalene in the presence of 10 mol% MOF-808 at 45 degrees C using only a fluorescent lamp. MOF-808 can be recycled up to 5 times with no loss in catalytic activity. A proof-of-principle substrate scope demonstrates the potential utility for aromatic and aliphatic substrates. (C) 2021 Elsevier Ltd. All rights reserved.

Product Details of 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Rabon, AM; Doremus, JG; Young, MC 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

Recently I am researching about ORGANIC-REACTIONS; IONIC LIQUID; BENZOTHIAZOLES; BENZIMIDAZOLES; BENZOXAZOLES; INHIBITORS; PROTOCOL, Saw an article supported by the Department of Chemistry, University of CalcuttaUniversity of Calcutta. Published in ORIENTAL SCIENTIFIC PUBL CO in BHOPAL ,Authors: Datta, A. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde. Formula: C8H8O2

In this work, one pot, simple and environmentally benign effective synthesis of 2-substituted benzothiazole and benzothiazoline derivatives are described in presence of PFPAT (pentafluorophenylammonium triflate) catalyst in water successfully. A series of benzothiazole derivative were synthesized by the reaction between 2-aminothiophenol and various aldehydes in good yields. Recyclability of the catalyst is observed for four times without loss of its activity in aqueous medium.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Datta, A or concate me.. Formula: C8H8O2

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

I found the field of Chemistry very interesting. Saw the article An uncoordinated tertiary nitrogen based tricarboxylate calcium network with Lewis acid-base dual catalytic sites for cyanosilylation of aldehydes published in 2021.0. SDS of cas: 123-11-5, Reprint Addresses Zhang, XM (corresponding author), Shanxi Normal Univ, Minist Educ, Key Lab Magnet Mol & Magnet Informat Mat, Inst Chem & Culture,Sch Chem & Mat Sci, Linfen 041004, Shanxi, Peoples R China.. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde

The design and utilization of dual sites for synergistic catalysts has been recognised as an efficient method towards high-efficiency catalysis in the cyanosilylation of aldehydes, which gives key intermediates for the synthesis of a number of valuable natural and pharmaceutical compounds. However, most of the reported dual-site catalysts for this reaction were homogeneous, accompanied by potential deactivation through internal complexation of the dual sites. Herein, by the rational selection of an uncoordinated tertiary nitrogen based tricarboxylic ligand (tris[(4-carboxyl)-phenylduryl]amine, H(3)TCBPA), a new three-dimensional calcium-based metal-organic framework (MOF), Ca-3(TCBPA)(2)(DMA)(2)(H2O)(2) (1, where TCBPA = ionized tris[(4-carboxyl)-phenylduryl]amine and DMA = N,N-dimethylacetamide), possessing accessible dual catalytic sites, Lewis-basic N and Lewis-acidic Ca, has been designed and constructed by a one-pot solvothermal reaction. As expected, 1 is capable of dually and heterogeneously catalysing the cyanosilylation of aldehydes at room temperature, and can be reused for at least 6 runs with a maximum turnover number (TON) of 1301, which is superior to most reported cases. Additionally, 1 shows CO2 adsorption ability and conversion with epoxides, which is beneficial for the establishment of a sustainable society.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Wang, YX; Wang, HM; Meng, P; Song, DX; Hou, JJ; Zhang, XM or concate me.. 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

Name: 4-Methoxybenzaldehyde. Authors Vetter, AC; Gilheany, DG; Nikitin, K in AMER CHEMICAL SOC published article about in [Vetter, Anna C.; Gilheany, Declan G.; Nikitin, Kirill] Univ Coll Dublin, Sch Chem, Dublin 4, Ireland in 2021.0, Cited 64.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Despite common perception, the use of strong bases in Wittig chemistry is utterly unnecessary: we report a series of novel ion-pair phosphonium carboxylate reagents which are essentially storable ylides. These reagents are straightforwardly prepared in excellent yields, and their fluxional nature permits clean olefination of a broad range of aldehydes and even hemiacetals.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Vetter, AC; Gilheany, DG; Nikitin, K or concate me.. Name: 4-Methoxybenzaldehyde

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: C8H8O2. Song, DW; Liu, GL; Xue, MY; Qiu, TX; Wang, H; Shan, LP; Liu, L; Chen, J in [Song, Da-Wei; Qiu, Tian-Xiu; Wang, Huan; Shan, Li-Peng; Liu, Lei; Chen, Jiong] Ningbo Univ, State Key Lab Managing Biot & Chem Threats Qual &, Ningbo 315211, Peoples R China; [Song, Da-Wei; Qiu, Tian-Xiu; Wang, Huan; Shan, Li-Peng; Liu, Lei; Chen, Jiong] Ningbo Univ, Sch Marine Sci, Lab Biochem & Mol Biol, Meishan Campus, Ningbo 315832, Peoples R China; [Song, Da-Wei; Qiu, Tian-Xiu; Wang, Huan; Shan, Li-Peng; Liu, Lei; Chen, Jiong] Ningbo Univ, Key Lab Appl Marine Biotechnol, Minist Educ, Meishan Campus, Ningbo 315832, Peoples R China; [Liu, Guang-Lu] Zhoukou Normal Univ, Sch Chem & Chem Engn, Zhoukou 466001, Peoples R China; [Xue, Ming-Yang] Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Wuhan 430223, Peoples R China published In vitro and in vivo evaluation of antiviral activity of a phenylpropanoid derivative against spring viraemia of carp virus in 2021, Cited 47. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

Phenylpropanoids, common natural compounds, possess many different biological activities such as antioxidant, anti-inflammatory and antiviral. Spring viraemia of carp virus (SVCV) can cause a high mortality in common carp (Cyprinus carpio). However, there are currently no licenced drugs that effectively cure this disease. In this study, we designed and synthesized a phenylpropanoid derivative 4-(4-methoxyphenyl)-3,4-dihydro-2H-chromeno[4,3-d]pyrimidine-2,5(1 H)-dione (E2), and explored the antiviral effect against SVCV in vitro and in vivo. Up to 25 mg/L of E2 significantly inhibited the expression levels of SVCV protein genes in the epithelioma papulosum cyprini (EPC) cell line by a maximum inhibitory rate of >90%. As expected, E2 remarkably declined the apoptotic of SVCV-infected cells and suppressed potential enhancement of the mitochondrial membrane potential (Delta Psi m), these data implied that E2 could protect mitochondria from structural damage in response to SVCV. Meanwhile, E2 was added to EPC cells under four different conditions: time-of-addition, time-of-removal, pre-treatment of viruses and pre-treatment of cells indicated that E2 may block the post-entry transport process of the virus. Additionally, the up-regulation of six interferon (IFN)-related genes also demonstrated that E2 indirectly activated IFNs for the clearance of SVCV in common carp. Drug cure effect showed that treatment with E2 at 0.5 d post infection (dpi) is more effective than at 0, 1 or 2 dpi. Most importantly, intraperitoneal therapy of E2 markedly improved common carp survival rate and reduced virus copies in body. Therefore, the E2 has potential to be developed into a novel anti-SVCV agent.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Song, DW; Liu, GL; Xue, MY; Qiu, TX; Wang, H; Shan, LP; Liu, L; Chen, J or concate me.. Formula: C8H8O2

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

Computed Properties of C8H8O2. In 2021 J IRAN CHEM SOC published article about ONE-POT SYNTHESIS; GREEN SYNTHESIS; IRRADIATION; CHLORIDE in [Azimzadeh-Sadeghi, Setareh] Islamic Azad Univ, Dept Chem, Sci & Res Branch, Tehran, Iran; [Yavari, Issa] Tarbiat Modares Univ, Dept Chem, Tehran, Iran in 2021, Cited 30. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

A novel deep eutectic solvent system was prepared by mixing choline chloride as a hydrogen-bond acceptor with 2,2-bis(hydroxymethyl)propane-1,3-diol (pentaerythritol) as a hydrogen-bond donor. This green solvent was used for the one-pot synthesis of pyran and chromene derivatives from aromatic aldehydes, 1,3-dicarbonyl compounds, and malononitrile. The solvent was readily recycled and can be reused three times without significant loss of activity or mass. This procedure offers advantages such as environmental friendliness, shorter reaction times, and higher yields.

Computed Properties of C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Azimzadeh-Sadeghi, S; Yavari, I 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

Quality Control of 4-Methoxybenzaldehyde. Authors Mu, QQ; Nie, YX; Li, H; Bai, XF; Liu, XW; Xu, Z; Xu, LW in ROYAL SOC CHEMISTRY published article about in [Mu, Qiu-Qi; Liu, Xue-Wei] Northwestern Polytech Univ, Inst Adv Synth IAS, Xian 710072, Peoples R China; [Mu, Qiu-Qi; Liu, Xue-Wei] Yangtze River Delta Res Inst NPU, Taicang 215400, Jiangsu, Peoples R China; [Mu, Qiu-Qi; Nie, Yi-Xue; Li, Hang; Bai, Xing-Feng; Xu, Zheng; Xu, Li-Wen] Hangzhou Normal Univ, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Peoples R China; [Mu, Qiu-Qi; Nie, Yi-Xue; Li, Hang; Bai, Xing-Feng; Xu, Zheng; Xu, Li-Wen] Hangzhou Normal Univ, Key Lab Organosilicon Mat Technol Zhejiang Prov, Hangzhou 311121, Peoples R China; [Mu, Qiu-Qi; Bai, Xing-Feng; Xu, Li-Wen] Univ Chinese Acad Sci UCAS, State Key Lab Oxo Synth & Select Oxidat, Suzhou Res Inst SRI, Lanzhou Inst Chem Phys LICP, Lanzhou 730000, Peoples R China; [Liu, Xue-Wei] Nanyang Technol Univ, Div Chem & Biol Chem, Sch Phys & Math Sci, Singapore 637371, Singapore in 2021.0, Cited 36.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A highly enantioselective kinetic resolution of sterically hindered benzylamines has been achieved for the first time through transition-metal-catalyzed oxidative carbonylation, in which the new KR strategy offered a new approach to afford chiral isoindolinones (er up to 97 : 3) and the origin of chemoselectivity and stereoselectivity was confirmed by density functional theory (DFT) calculations.

Quality Control of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Mu, QQ; Nie, YX; Li, H; Bai, XF; Liu, XW; Xu, Z; Xu, LW 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

Application In Synthesis of 4-Methoxybenzaldehyde. Authors Hussein, AHM; Khames, AA; El-Adasy, AA; Atalla, AA; Abdel-Rady, M; Hassan, MIA; Abou-Salim, MA; Elshaier, YAMM; Barakat, A in MDPI published article about in [Hussein, Abdel Haleem M.; Khames, Ahmed A.; El-Adasy, Abu-Bakr A.; Atalla, Ahmed A.] Al Azhar Univ, Dept Chem, Fac Sci, Assiut 71524, Egypt; [Abdel-Rady, Mohamed] Assiut Univ, Dept Chem, Fac Sci, Assiut 71516, Egypt; [Hassan, Mohamed I. A.] Al Azhar Univ, Dept Pharmacol & Toxicol, Fac Pharm, Assiut 71524, Egypt; [Abou-Salim, Mahrous A.] Al Azhar Univ, Dept Pharmaceut Organ Chem, Fac Pharm, Assiut 71524, Egypt; [Elshaier, Yaseen A. M. M.] Univ Sadat City, Dept Organ & Med Chem, Fac Pharm, Menoufia 32958, Egypt; [Barakat, Assem] King Saud Univ, Dept Chem, Coll Sci, POB 2455, Riyadh 11451, Saudi Arabia; [Barakat, Assem] Alexandria Univ, Dept Chem, Fac Sci, Alexandria 21321, Egypt in 2021, Cited 34. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The elaboration of new small molecules that target phosphodiesterase enzymes (PDEs), especially those of type 5 (PDE5), is an interesting and emerging topic nowadays. A new series of heterocycle-based aminothiazoles were designed and synthesized from the key intermediate, 3-oxo-N-(thiazol-2-yl)butanamide (a PDE5 inhibitor that retains its amidic function), as an essential pharmacophoric moiety. The PDE5 inhibitors prevent the degradation of cyclic guanosine monophosphate, thereby causing severe hypotension as a marked side effect. Hence, an in vivo testing of the target compounds was conducted to verify its relation with arterial blood pressure. Utilizing sildenafil as the reference drug, Compounds 5, 10a, and 11b achieved 100% inhibitions of PDE5 without significantly lowering the mean arterial blood pressures (115.95 +/- 2.91, 110.3 +/- 2.84, and 78.3 +/- 2.57, respectively). The molecular docking study revealed that the tested compounds exhibited docking poses that were similar to that of sildenafil (exploiting the amide functionality that interacted with GLN:817:A). The molecular shape and electrostatic similarity revealed a comparable physically achievable electrostatic potential with the reference drug, sildenafil. Therefore, these concomitant results revealed that the tested compounds exerted sildenafil-like inhibitory effects (although without its known drawbacks) on blood circulation, thus suggesting that the tested compounds might represent a cornerstone of beneficial drug candidates for the safe treatment for erectile dysfunction.

Application In Synthesis of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Hussein, AHM; Khames, AA; El-Adasy, AA; Atalla, AA; Abdel-Rady, M; Hassan, MIA; Abou-Salim, MA; Elshaier, YAMM; Barakat, A 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

Xue, KS; Sun, GX; Zhang, YZ; Chen, XB; Zhou, Y; Hou, JJ; Long, HL; Zhang, ZJ; Lei, M; Wu, WY in [Xue, Kangsheng] Changchun Univ Chinese Med, Coll Pharm, Changchun, Peoples R China; [Sun, Guoxiang] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng, Jiangsu, Peoples R China; [Zhang, Yanzhi; Chen, Xubing] Dali Univ, Coll Pharm, Dali, Peoples R China; [Zhou, Yang; Hou, Jinjun; Long, Huali; Zhang, Zijia; Lei, Min; Wu, Wanying] Chinese Acad Sci, Shanghai Res Ctr Modernizat Tradit Chinese Med, Shanghai Inst Mat Med, Natl Engn Lab TCM Standardizat Technol, Shanghai, Peoples R China; [Zhou, Yang; Hou, Jinjun; Long, Huali; Zhang, Zijia; Lei, Min; Wu, Wanying] Univ Chinese Acad Sci, Beijing, Peoples R China published A new method for the synthesis of chalcone derivatives promoted by PPh3/I(2)under non-alkaline conditions in 2021, Cited 61. Recommanded Product: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

A straightforward and general method has been developed for the synthesis of chalcone derivatives by a Claisen-Schmidt reaction in the presence of PPh3/I-2 in 1,4-dioxane under reflux temperatures. With the condensation of the aromatic ketone and aldehyde occurring at non-strongly alkaline conditions, our proposed method significantly expands the range of applicable substrates, especially for groups that are unstable under alkaline conditions.

Recommanded Product: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Xue, KS; Sun, GX; Zhang, YZ; Chen, XB; Zhou, Y; Hou, JJ; Long, HL; Zhang, ZJ; Lei, M; Wu, WY 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

Application In Synthesis of 4-Methoxybenzaldehyde. Authors Asressu, KH; Chan, CK; Wang, CC in AMER CHEMICAL SOC published article about in [Asressu, Kesatebrhan Haile; Chan, Chieh-Kai; Wang, Cheng-Chung] Acad Sinica, Inst Chem, Taipei 115, Taiwan in 2021.0, Cited 67.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

We developed a facile and green one-pot synthetic method for substituted 1,3,5-triaryl-1,5-diketones by Claisen-Schmidt condensation following Michael addition reaction of aryl ketones and aryl aldehydes under a transition-metal-free condition. This convenient one-pot synthetic strategy has several advantages, including being transition-metal-free, having no extra additives or reagents, having a broad substrate scope, having a high isolated yield, having a minimum amount of base employment, having a shorter reaction time, use of cheap starting materials, cost-effectiveness, and being environment friendly. Some of the chemical structures of 1,5-diketones were confirmed by X-ray single-crystal diffraction analysis. The application of 1,5-diketones was demonstrated in the preparation of 2,4,6-triaryl pyridine derivatives under a catalyst-free system using ammonium acetate as a nitrogen source.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Asressu, KH; Chan, CK; Wang, CC or concate me.. Application In Synthesis of 4-Methoxybenzaldehyde

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