Month: December 2021

Name: Benzyl Alcohol. In 2019.0 MACROMOLECULES published article about RING-OPENING POLYMERIZATION; POLYPHOSPHOESTER IONOMERS; POLY(ETHYLENE GLYCOL); BLOCK-COPOLYMERS; POLYMERS; ACID; POLYPHOSPHORAMIDATE; POLY(PHOSPHONATE)S; POLYTHIOESTERS; EFFICIENT in [Liu, Yi; Bejjanki, Naveen Kumar; Jiang, Wei; Zhao, Yangyang; Wang, Li; Sun, Xun; Tang, Xinfeng; Liu, Hang; Wang, Yucai] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Sch Life Sci, Div Mol Med,CAS Key Lab Innate Immun & Chron Dis, Hefei 230026, Anhui, Peoples R China in 2019.0, Cited 42.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.

We reported the preparation of well-defined poly(thionophosphoester)s as oxidation-responsive materials that undergo peroxide-triggered degradation. The polymers were synthesized via the controlled ring-opening polymerization of cyclic thionophosphoesters initiated with hydroxyl terminal small molecule and macromolecular initiators and catalyzed with 1,5,7-triazabicyclo[4.4.0]dec-5-ene in tetrahydrofuran at room temperature. The resulting poly-(thionophosphoester)s were characterized in detail by NMR spectroscopy and size exclusion chromatography. Polymerization of cyclic oxophosphoester (P=O) monomers exhibited broad molecular weight distribution and severe side reactions, while narrow molecular weight distribution ((D) over bar (M) similar to 1.1) was achieved without significant transesterifications using thionophosphoester (P=S) monomers. The reaction kinetics of thionophosphoester monomers were in agreement with living polymerization characteristics. Furthermore, by replacing P=O bond by P=S, the polymers changed from hydrophilic to hydrophobic. These well-controlled sulfur-containing polymers are more resistant to hydrolytic degradation but undergo peroxide-triggered degradation. Poly(thionophosphoester)s are thus promising in the field of biomedical materials.

Name: Benzyl Alcohol. About Benzyl Alcohol, If you have any questions, you can contact Liu, Y; Bejjanki, NK; Jiang, W; Zhao, YY; Wang, L; Sun, X; Tang, XF; Liu, H; Wang, YC 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

In 2021 RSC ADV published article about ONE-POT SYNTHESIS; RECOVERABLE NANO-CATALYST; FACILE SYNTHESIS; IONIC LIQUID; RECYCLABLE CATALYST; NATURAL PHOSPHATE; HIGHLY EFFICIENT; GREEN CHEMISTRY; SULFONIC-ACID; NANOPARTICLES in [Kargar, Pouya Ghamari; Bagherzade, Ghodsieh] Univ Birjand, Fac Sci, Dept Chem, Birjand 97175615, Iran; [Eshghi, Hossein] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad, Razavi Khorasan, Iran in 2021, Cited 77. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Recommanded Product: 123-11-5

In this work, the new trinuclear manganese catalyst defined as Fe3O4@NFC@NNSM-Mn(iii) was successfully manufactured and fully characterized by different techniques, including FT-IR, XRD, TEM, SEM, EDX, VSM, and ICP analysis. There have been reports of the use of magnetic catalysts for the synthesis of xanthine derivatives. The critical potential interest in the present method include short reaction time, high yields, recyclability of the catalyst, easy workup, and the ability to sustain a variety of functional groups, which give economical as well as ecological rewards. Also, the synthesized catalyst was used as a recyclable trinuclear catalyst in alcohol oxidation reactions at 40 degrees C. The magnetic catalyst activity of Fe3O4@NFC@NNSM-Mn(iii) could be attributed to the synergistic effects of the catalyst Fe3O4@NFC@NNS-Mn(iii) with melamine. Employing a sustainable and safe low temperature, using an eco-friendly solvent, no need to use any additive, and long-term stability and magnetic recyclability of the catalyst for at least six successive runs are the advantages of the current protocol towards green chemistry. This protocol is a benign, environmentally friendly method for heterocycle synthesis.

Recommanded Product: 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Kargar, PG; Bagherzade, G; Eshghi, H 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

Recommanded Product: m-Methoxyphenol. In 2021.0 COMPUT THEOR CHEM published article about RADICAL-MOLECULE REACTIONS; TRANSITION-STATE MODEL; THERMAL-DECOMPOSITION; LIGNOCELLULOSIC BIOMASS; ANISOLE PYROLYSIS; FLAME STRUCTURE; RATE CONSTANTS; KINETICS; OH; MECHANISM in [Wang, Quan-De; Sun, Mao-Mao] China Univ Min & Technol, Low Carbon Energy Inst, Xuzhou 221008, Jiangsu, Peoples R China; [Wang, Quan-De; Sun, Mao-Mao] China Univ Min & Technol, Sch Chem Engn, Xuzhou 221008, Jiangsu, Peoples R China; [Liang, Jinhu] North Univ China, Sch Environm & Safety Engn, Taiyuan 030051, Peoples R China in 2021.0, Cited 62.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

The growing interest in the use of bio-oils requires a detailed understanding of its combustion chemical kinetics. Bio-oils contain a large variety of oxygenated organic species, in which substituted phenolic compounds are among the most significant fractions. Hence, accurate assessment of key reaction rate constants and systematically investigated the structural effect on the reactivity are critical. This work reports a systematic theoretical study of the hydrogen abstraction reactions from phenol, anisole, o-guaiacol, m-guaiacol, and p-guaiacol, which are considered as reference components in bio-oil surrogates. The hydrogen abstraction reactions by five different radicals (H/CH3/O(P-3)/OH/HO2) are investigated at ROCBS-QB3//M06-2X/cc-pVTZ level. The highpressure limit rate constants are computed via transition state theory with Eckart tunnelling and the 1-D hindered rotor approximation. Comparisons of site-specific hydrogen abstractions from the studied species with other related species are performed to understand the effects of the aromatic ring and side-chain substituent on hydrogen abstractions.

Recommanded Product: m-Methoxyphenol. Welcome to talk about 150-19-6, If you have any questions, you can contact Wang, QD; Sun, MM; Liang, JH 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

Authors Rao, TN; Krishnarao, N; Ahmed, F; Alomar, SY; Albalawi, F; Mani, P; Aljaafari, A; Parvatamma, B; Arshi, N; Kumar, S in MDPI published article about in [Rao, Tentu Nageswara; Krishnarao, Nalla] Krishna Univ, Dept Chem, Machilipatnam 521001, Andhra Pradesh, India; [Ahmed, Faheem; Aljaafari, Abdullah; Kumar, Shalendra] King Faisal Univ, Dept Phys, Coll Sci, Al Hufuf 31982, Al Ahsa, Saudi Arabia; [Alomar, Suliman Yousef] King Saud Univ, Zool Dept, Coll Sci, Doping Res Chair, Riyadh 11451, Saudi Arabia; [Albalawi, Fadwa] King Saud Univ, Zool Dept, Coll Sci, Riyadh 11451, Saudi Arabia; [Mani, Panagal] Dept Biotechnol, Annai Coll Arts Sci, Kumbakonam 612503, Tamil Nadu, India; [Parvatamma, Botsa] GayathriPG Courses, Dept Organ Chem, Gotlam, Vizianagaram 530045, India; [Arshi, Nishat] King Faisal Univ, Dept Basic Sci, Preparatory Year Deanship, Al Hufuf, Al Ahsa, Saudi Arabia; [Kumar, Shalendra] Univ Petr & Energy Studies, Sch Engn, Dept Phys, Dehra Dun 248007, Uttarakhand, India in 2021, Cited 37. Quality Control of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A simple and highly efficient protocol for the synthesis of derivatives 7, 7-dimethyl-4-phenyl-2-thioxo-2, 3, 4, 6, 7, 8-hexahydro-1H-quinazoline-5-one from 5, 5-dimethyl cyclohexane-1, 3-dione (4a-4h) (dimedone) has been described. The aryl aldehydes were substituted with thiourea in the presence of synthesized zinc ferrite nanocatalyst, which increased the yield under reflux through condensation, followed by cyclization to give desired products. The other advantages are that it is eco-friendly and economically affordable for large-scale production. Structural validation and characterization of all the newly synthesized compounds were evaluated by spectral analysis (mass spectrometry, proton nuclear magnetic resonance ((HNMR)-H-1), and Carbon-13 nuclear magnetic resonance((CNMR)-C-13)spectroscopies. The structure of antibacterial and antifungal assays was performed with the newly synthesized compounds. The antimicrobial activity of title compounds possessing electron-withdrawing groups such as (4e-4h) (Cl, Br, and cyano group) exhibited more active potential than the electron-donating groups, C6H5,4-C6H4, 3-OC2H5-4OH-C6H3, etc., (4a-4d) containing moiety.

Quality Control of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Rao, TN; Krishnarao, N; Ahmed, F; Alomar, SY; Albalawi, F; Mani, P; Aljaafari, A; Parvatamma, B; Arshi, N; Kumar, 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

Dandia, A; Saini, P; Chithra, MJ; Vennapusa, SR; Parewa, V in [Dandia, Anshu; Saini, Pratibha; Parewa, Vijay] Univ Rajasthan, Ctr Adv Studies, Dept Chem, Jaipur, Rajasthan, India; [Chithra, M. J.; Vennapusa, Sivaranjana Reddy] Indian Inst Sci Educ & Res Thiruvananthapuram, Maruthamala PO, Thiruvananthapuram 695551, Kerala, India published Catalyst- and acid-free Markovnikov hydration of alkynes in a sustainable H2O/ethyl lactate system in 2021, Cited 62. Safety of 4′-Hydroxyacetophenone. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

An efficient and sustainable protocol for the hydration of alkynes has been developed under metal/acid/catalyst/ ligand-free conditions in a water/ethyl lactate mixture. The hydrogen-bond network in the ethyl lactate and water mixture plays a crucial and decisive role in activating the alkynes for hydration to afford the corresponding methyl ketones. This strategy gives the Markovnikov (ketone) addition product selectively over other possible products. The essential role of hydrogen bonding has been confirmed by experimental and theoretical techniques. A probable mechanism has been suggested by various control tests. The efficacy of the method has been further explored for the competent production of value-added alpha,beta-unsaturated carbonyl compounds through the reaction of aldehydes with alkynes as ketonic surrogates. The environmentally benign hydration method takes place under mild conditions, has broad functional-group compatibility, and uses the ethyl lactate/water (1:3) medium as a green alternative in the absence of any hazardous, harmful, or expensive substances. (C) 2021 Elsevier B.V. All rights reserved.

Safety of 4′-Hydroxyacetophenone. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Dandia, A; Saini, P; Chithra, MJ; Vennapusa, SR; Parewa, V 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

Recommanded Product: 120-14-9. Authors Liu, Y; Zhang, Y; Huang, QW; Gou, CA; Li, QZ; Dai, QS; Leng, HJ; Li, JL in WILEY-V C H VERLAG GMBH published article about in [Liu, Yue; Zhang, Ying; Huang, Qian-Wei; Gou, Chuan; Li, Qing-Zhu; Dai, Qing-Song; Leng, Hai-Jun; Li, Jun-Long] Chengdu Univ, Sichuan Ind Inst Antibiot, Sch Pharm, Antibiot Res & Reevaluat Key Lab Sichuan Prov, Chengdu 610106, Peoples R China in 2021.0, Cited 77.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9

Asymmetric construction of pharmacologically interesting tetrahydrofuranyl spirooxindole frameworks has been achieved through organocatalytic [3+2] annulations of the readily available 3-hydroxyoxindoles and pyrrolidone-derived cyclic ketolactams. A variety of chiral spiro tetrahydrofuranyl products, which contain four contiguous stereocenters including two tetrasubstituted carbon centers, have been rapidly synthesized with remarkable results (up to 99% yield, >95:5 dr, and 99:1 er). Synthetic derivatization of the hemiketal moiety enables the installation of various halogen atoms into the structurally complex molecules in a stereospecific manner. Preliminary screening of anticancer bioactivity was performed, and 4 w showed obvious inhibitory capacity to the proliferation on a panel of cancer cell lines.

Recommanded Product: 120-14-9. Bye, fridends, I hope you can learn more about C9H10O3, If you have any questions, you can browse other blog as well. See you lster.

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 2021 EUR J ORG CHEM published article about METAL-FREE; NUCLEOPHILIC TRIFLUOROMETHYLATION; ASYMMETRIC-SYNTHESIS; KETONES; AMINES; IMINES in [Mehta, Jatin; Aryal, Puspa; Prakash Reddy, V.] Missouri Univ Sci & Technol, Dept Chem, Rolla, MO 65409 USA in 2021, Cited 39. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Recommanded Product: 4-Methoxybenzaldehyde

The C(sp(2)-H)-trifluoromethylation of hydrazones would give access to the alpha-trifluoromethylated hydrazones that can serve as intermediates in the synthesis of pharmaceutically interesting fluorinated compounds. Herein, we demonstrate the Cu-catalyzed C(sp(2)-H)-trifluoromethylation of the aldehyde hydrazones using the readily available and cost effective Langlois reagent (sodium trifluoromethanesulfinate). This reaction is broadly applicable to a series of aromatic aldehyde N-aminomorpholine hydrazones to give the corresponding C(sp(2))-trifluoromethyl hydrazones in moderate to high yields. The reaction generally tolerates a series of electron-releasing as well as electron-withdrawing substituents on the aromatic ring.

Recommanded Product: 4-Methoxybenzaldehyde. Welcome to talk about 123-11-5, If you have any questions, you can contact Mehta, J; Aryal, P; Reddy, VP 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

Bettencourt, AP; Castro, M; Silva, JP; Fernandes, F; Coutinho, OP; Sousa, MJ; Proenca, MF; Areias, FM in [Bettencourt, Ana P.; Fernandes, Francisco; Proenca, Maria Fernanda; Areias, Filipe M.] Univ Minho, Dept Chem, Campus Gualtar, P-4710057 Braga, Portugal; [Castro, Marian] Univ Santiago de Compostela, BioFarma Res Grp, Ctr Res Mol Med & Chron Dis CiMUS, Ave Barcelona 22, Santiago De Compostela 15782, Spain; [Silva, Joao P.; Coutinho, Olga P.] Univ Minho, Dept Biol, Campus Gualtar, P-4710057 Braga, Portugal; [Sousa, Maria J.; Areias, Filipe M.] Univ Minho, CBMA Ctr Mol & Environm Biol, Dept Biol, Campus Gualtar, P-4710057 Braga, Portugal; [Areias, Filipe M.] Yachay Tech Univ, Sch Chem Sci & Engn, Yachay City Of Knowledge 100650, Urcuqui, Ecuador published Phenolic Imidazole Derivatives with Dual Antioxidant/Antifungal Activity: Synthesis and Structure-Activity Relationship in 2019.0, Cited 33.0. Safety of 3-Hydroxybenzaldehyde. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Background: Previous publications show that the addition of a phenolic antioxidant to an antifungal agent, considerably enhances the antifungal activity. Objective: Synthesis of novel compounds combining phenolic units with linear or cyclic nitrogencontaining organic molecules with antioxidant/antifungal activity using methodologies previously developed in the group. Methods: Several N- [1,2-dicyano-2- (arylidenamino) vinyl]-O-alkylformamidoximes 3 were synthesized and cyclized to 4,5-dicyano-N- (N’-alcoxyformimidoyl)-2-arylimidazoles 4 upon reflux in DMF, in the presence of manganese dioxide or to 6-cyano-8-arylpurines 5 when the reagent was refluxed in acetonitrile with an excess of triethylamine. These compounds were tested for their antioxidant activity by cyclic voltammetry, DPPH radical (DPPH.) assay and deoxyribose degradation assay. The minimum inhibitory concentration (MIC) of all compounds was evaluated against two yeast species, Saccharomyces cerevisiae and Candida albicans, and against bacteria Bacillus suhtill’s (Gram-positive) and Escherichia call (Gram negative). Their cytotoxicity was evaluated in fibroblasts. Results: Among the synthetised compounds, five presented higher antioxidant activity than reference antioxidant Trolox and from these compounds, four presented antifungal activity without toxic effects in fibroblasts and bacteria. Conclusion: Four novel compounds presented dual antioxidant/antifimgal activity at concentrations that are not toxic to bacteria and fibroblasts. The active molecules can be used as an inspiration for further studies in this area.

Safety of 3-Hydroxybenzaldehyde. Welcome to talk about 100-83-4, If you have any questions, you can contact Bettencourt, AP; Castro, M; Silva, JP; Fernandes, F; Coutinho, OP; Sousa, MJ; Proenca, MF; Areias, FM 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

Formula: C8H8O2. Authors Mansour, SY; Sayed, GH; Marzouk, MI; Shaban, SS in TAYLOR & FRANCIS INC published article about in [Mansour, S. Y.; Sayed, G. H.; Marzouk, M. I.; Shaban, S. S.] Ain Shams Univ, Fac Sci, Chem Dept, Heterocycl Synthet Lab, Cairo, Egypt in 2021.0, Cited 22.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The 2-Aminonicotinonitrile derivative was reacted with different bi-functional reagents such as formamide, thiourea, acetic anhydride, and phthalic anhydride under optimized conditions to give pyrimidine, thiourea, acetamide, and isoindoline derivatives, respectively, When it was treated with active methylene reagents as malononitrile, phenacyl bromide, and ethyl bromoacetate under varied experimental modulation, it afforded 1, 8-naphthyridine, ethyl, and methylamino nicotinonitrile derivatives, respectively. Also, it was reacted with p-toluene sulfonyl chloride, chloroacetyl chloride, and benzoyl chloride to give sulfonamide, 2-chloro-N-acetamide, and benzamide derivatives, respectively. Likewise, it was reacted with diethyl malonate, ethyl cyanoacetate, and cyano acetic acid to give ethylpropanoate, naphthyridine, and cyano acetamide derivatives, respectively. However, treatment of ethylpropanoate and cyano acetamide derivatives with hydrazine hydrate gave pyrazole and 5-amino-pyrazole nicotinonitrile derivatives, respectively. In addition, it was reacted with p-anisaldehyde, phenyl isocyanate, and triethyl orthoformate to give benzylamino nicotinonitrile, phenyl urea, and N-formamide derivatives, respectively. Furthermore, it was reacted with nitrous acid then coupled with aniline; it was also reacted with isatine and 1,3- dibromo propane to give oxoindoline derivative, and the dimer. Elemental analyses, together with spectroscopic data including IR, H-1-NMR in addition to C-13-NMR and mass spectra submit proofs for the chemical structures for all compounds. [GRAPHICS]

Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Mansour, SY; Sayed, GH; Marzouk, MI; Shaban, SS 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 Carbamoyl-N-aryl-imine-urea: a new framework to obtain a putative leishmanicidal drug-candidate published in 2020.0, Reprint Addresses Lima, LM (corresponding author), Univ Fed Rio De Janeiro UFRJ, Lab Avaliacao & Sintese Subst Bioativas LASSBio, Inst Nacl Ciencia & Tecnol Farmacos & Medicamento, CCS, POB 68023, BR-21941902 Rio De Janeiro, RJ, Brazil.; Lima, LM (corresponding author), Univ Fed Rio de Janeiro, Inst Quim, Programa Posgrad Quim, BR-21941909 Rio de Janeiro, RJ, Brazil.; Alexandre-Moreira, MS (corresponding author), Univ Fed Alagoas UFAL, Inst Ciencias Biol & Sande, Lab Farmacol & Imunol, BR-57072900 Maceio, AL, Brazil.. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde.

Leishmaniasis is a neglected parasitic disease, and current treatment includes limitations of toxicity, variable efficacy, high costs and inconvenient doses and treatment schedules. Therefore, new leishmanicidal drugs are still an unquestionable medical need. In this paper we described the design conception of a new framework, the carbamoyl-N-aryl-imine-urea, to obtain putative leishmanicidal drug-candidates. Compounds 9a-e and 10a-e were designed and synthesized and their leishmanicidal activity was studied in comparison to pentamidine, miltefosine and meglumine antimoniate. The conformational profile of the new carbamoyl-N-aryl-imine-urea framework was investigated by X-ray diffraction studies, using compound 9a as a model. The plasma stability of this putative peptide mimetic subunit was studied for compound 10e (LASSBio-1736). Among the congeneric series, LASSBio-1736 was identified as a new antileishmanial drug-candidate, displaying plasma stability, cytotoxicity against amastigote forms of L. amazonensis and L. braziliensis, and leishmanicidal activity in a cutaneous leishmaniasis murine model, without preliminary evidence of hepatic or renal toxicity.

Welcome to talk about 100-83-4, If you have any questions, you can contact Alves, MA; de Queiroz, AC; Leite, AB; Martins, FT; Doriguetto, AC; Barreiro, EJ; Alexandre-Moreira, MS; Lima, LM or send Email.. 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