CAS 3133-78-6
:Acide 3-méthylbenzo[b]thiophène-2-carboxylique
- 3-Methyl-1-benzothiophene-2-carboxylic acid
- Benzo[b]thiophene-2-carboxylic acid, 3-methyl-
- 3-Methyl-1-Benzothiophene-2-Carboxylate
- 3-Methylbenzothiophene-2-carboxylicacid
3-Methylbenzo[b]thiophene-2-carboxylic acid, 97%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C10H8O2SDegré de pureté :97%Masse moléculaire :192.243-Methylbenzo[b]thiophene-2-carboxylic acid
CAS :Formule :C10H8O2SDegré de pureté :97%Couleur et forme :SolidMasse moléculaire :192.23433-Methylbenzo[b]thiophene-2-carboxylic acid
CAS :3-Methylbenzo[b]thiophene-2-carboxylic acidDegré de pureté :97%Masse moléculaire :192.24g/mol3-Methylbenzo[b]thiophene-2-carboxylic acid
CAS :Formule :C10H8O2SDegré de pureté :95%Couleur et forme :Liquid, No data available.Masse moléculaire :192.233-Methylbenzo[b]thiophene-2-carboxylic acid
CAS :3-Methylbenzo[b]thiophene-2-carboxylic acid (MBTCA) is a heterocyclic compound that is an intermediate in the synthesis of 3-methylthiophene-2-carboxylic acid, a precursor to other drugs. MBTCA is an aerobic, nonpolar compound that has shown antimicrobial activity against some bacteria and fungi. It also has been shown to have practicality as a biomolecular probe for methyl groups in organic solvents. MBTCA can be synthesized by nitration of benzene in the presence of sulfur and sulfoxides. This reaction produces nitrobenzene, which can then be oxidized by potassium permanganate or hydrogen peroxide to produce MBTCA. The most common isomer of MBTCA is 2-(3,5-dimethoxybenzylidene)tetrahydrofuran, with three methyl groups on the
Formule :C10H8O2SDegré de pureté :Min. 95%Masse moléculaire :192.23 g/mol




