CAS 34058-50-9
:1H-Indole-4-carboxylic acid, 2-methyl-
Description:
1H-Indole-4-carboxylic acid, 2-methyl- (CAS 34058-50-9) is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a carboxylic acid functional group at the 4-position and a methyl group at the 2-position of the indole ring. It is typically a white to off-white solid and is soluble in polar solvents, reflecting its polar functional groups. The presence of the carboxylic acid group allows for potential acid-base reactions and hydrogen bonding, which can influence its reactivity and interactions with other molecules. This compound may be of interest in various fields, including medicinal chemistry and biochemistry, due to its structural similarity to biologically active compounds. Its derivatives can exhibit a range of biological activities, making it a subject of research in drug development and synthesis. Overall, 1H-Indole-4-carboxylic acid, 2-methyl- is a versatile compound with potential applications in various chemical and pharmaceutical contexts.
Formula:C10H9NO2
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Found 3 products.
2-Methyl-1H-indole-4-carboxylic acid
CAS:Formula:C10H9NO2Purity:98%Color and Shape:SolidMolecular weight:175.18402-Methyl-1H-indole-4-carboxylic acid
CAS:<p>2-Methyl-1H-indole-4-carboxylic acid (2MICA) is a cyclic compound that is used in the synthesis of other compounds. It is obtained by reacting 2,3-dibromo-nitrobenzoic acid with sodium ethoxide in an alkaline solution. The yield of 2MICA can be increased by using catalytic acid anhydrides such as dimethyl sulphoxide or lactam. In the presence of reductive agents, 2MICA can be synthesized from the corresponding lactam or cyclised carboxylic acid.<br>2MICA reacts with sodium ethoxide to form a lactam and reduces 2-bromo-3-nitrobenzoic acid to yield 2MICA.</p>Formula:C10H9NO2Purity:Min. 95%Molecular weight:175 g/mol
