CAS 53995-82-7

Ethyl 4,6-dichloroindole-2-carboxylate

Description:

Ethyl 4,6-dichloroindole-2-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features two chlorine substituents at the 4 and 6 positions of the indole ring, contributing to its reactivity and potential biological activity. The presence of the ethyl ester group at the 2-carboxylate position enhances its solubility in organic solvents and may influence its pharmacological properties. Ethyl 4,6-dichloroindole-2-carboxylate is typically synthesized through specific organic reactions involving indole derivatives and chlorinating agents. It may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. As with many chlorinated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns. Proper safety protocols should be followed when working with this substance in laboratory settings.

Formula: C₁₁H₉Cl₂NO₂

InChI: InChI=1/C11H9Cl2NO2/c1-2-16-11(15)10-5-7-8(13)3-6(12)4-9(7)14-10/h3-5,14H,2H2,1H3

SMILES: CCOC(=O)c1cc2c(cc(cc2[nH]1)Cl)Cl

Synonyms:

• Ethyl 4,6-dichloro-1H-indole-2-carboxylate
• 4,6-dichloro-1H-Indole-2-carboxylic acid ethyl ester

1H-​Indole-​2-​carboxylic acid, 4,​6-​dichloro-​, ethyl ester

CAS: 53995-82-7

Formula: C₁₁H₉Cl₂NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 258.1007

Ref: IN-DA00I9MX

Ethyl 4,6-dichloro-1H-indole-2-carboxylate

CAS: 53995-82-7

Ethyl 4,6-dichloro-1H-indole-2-carboxylate

Purity: 95%

Molecular weight: 258.10g/mol

Ref: 54-OR8093

4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester

CAS: 53995-82-7

4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is a synthetic compound that functions as an agonist of the indole 2 receptor. It has been shown to have affinity for cortical and brain membranes, with a greater affinity for acidic regions of the membrane. 4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester is also capable of binding to the indole 2 receptor and activating it. The carboxyl group in this compound is substituted with benzene rings, which are connected by a moiety containing two carboxylic groups. 4,6-Dichloro-1H-indole-2-carboxylic acid ethyl ester was synthesised from 1H -indole acetic acid and chloroethane in four steps.

Formula: C₁₁H₉Cl₂NO₂

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 258.1 g/mol

Ref: 3D-FD56357

Ethyl 4,6-dichloro-1H-indole-2-carboxylate

CAS: 53995-82-7

Formula: C₁₁H₉Cl₂NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 258.1

Ref: 10-F040984