CAS 136831-13-5

1H-Indole-2-carboxylic acid, 4-methyl-, methyl ester

Description:

1H-Indole-2-carboxylic acid, 4-methyl-, methyl ester, with the CAS number 136831-13-5, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a carboxylic acid group at the 2-position and a methyl ester at the 4-position, contributing to its chemical reactivity and potential biological activity. The presence of the methyl group enhances its lipophilicity, which may influence its solubility and permeability in biological systems. Typically, compounds of this nature are studied for their pharmacological properties, as indole derivatives are known to exhibit a range of biological activities, including anti-inflammatory and antimicrobial effects. The compound's molecular structure allows for various functional group interactions, making it a candidate for further research in medicinal chemistry. Additionally, its synthesis and characterization can be achieved through standard organic synthesis techniques, and it may serve as an intermediate in the development of more complex pharmaceuticals.

Formula: C₁₁H₁₁NO₂

1H-Indole-2-carboxylic acid, 4-Methyl-, Methyl ester

CAS: 136831-13-5

Formula: C₁₁H₁₁NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 189.2105

Ref: IN-DA0012FO

4-Methyl-1H-indole-2-carboxylic acid methyl ester

CAS: 136831-13-5

4-Methyl-1H-indole-2-carboxylic acid methyl ester

Formula: C₁₁H₁₁NO₂

Purity: 95%

Color and Shape: beige solid

Molecular weight: 189.21g/mol

Ref: 54-OR346108

4-Methyl-1H-indole-2-carboxylic acid methyl ester

CAS: 136831-13-5

Formula: C₁₁H₁₁NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 189.214

Ref: 10-F047494

4-Methyl-1H-indole-2-carboxylic acid methyl ester

CAS: 136831-13-5

Nosiheptide is a thiopeptide antibiotic that is a mixture of (E) and (Z) isomers. It is effective against Gram-positive bacteria, such as staphylococci and streptococci, and Gram-negative bacteria, such as Escherichia coli and Pseudomonas aeruginosa. Nosiheptide binds to the 3-amino-4-chlorobenzoic acid in the bacterial cell wall by competitive inhibition. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. Lactone ring opens up, forming hydroxymethyl group which acts as hydrogen donor.

Formula: C₁₁H₁₁NO₂

Purity: Min. 95%

Molecular weight: 189.21 g/mol

Ref: 3D-LFA83113