Methyl 6-Amino-4-indolecarboxylate Hydrochloride

Methyl 6-Amino-4-indolecarboxylate Hydrochloride - Names and Identifiers

Name	METHYL 6-AMINO-4-INDOLECARBOXYLATE
Synonyms	METHYL 6-AMINO-4-INDOLECARBOXYLATE Methyl 6-aminoindole-4-carboxylate methyl 6-amino-1H-indole-4-carboxylate Methyl 6-aMino-1H-indole-4-carboxylate 6-AMINO-4-INDOLECARBOXYLIC ACID METHYL ESTER 6-AMINOINDOLE-4-CARBOXYLIC ACID METHYL ESTER 6-AMINO-1H-INDOLE-4-CARBOXYLIC ACID METHYL ESTER Methyl 6-Amino-4-indolecarboxylate Hydrochloride 1H-Indole-4-carboxylic acid, 6-aMino-, Methyl ester 1H-Indole-4-carboxylicacid,6-amino-,methylester(9CI)
CAS	103956-00-9
InChI	InChI=1/C10H10N2O2/c1-14-10(13)8-4-6(11)5-9-7(8)2-3-12-9/h2-5,12H,11H2,1H3

Methyl 6-Amino-4-indolecarboxylate Hydrochloride - Physico-chemical Properties

Molecular Formula	C10H10N2O2
Molar Mass	190.2
Density	1.339
Boling Point	429.8±25.0 °C(Predicted)
Flash Point	213.7°C
Vapor Presure	1.36E-07mmHg at 25°C
pKa	17.03±0.30(Predicted)
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature
Refractive Index	1.694

Methyl 6-Amino-4-indolecarboxylate Hydrochloride - Introduction

Methyl 6-aminoindole-4-carboxylate is an organic compound with the chemical formula C10H10N2O2. The following is a description of its nature, use, formulation and safety information:

Nature:
Methyl 6-aminoindole-4-carboxylate is a white to light yellow crystal or powder with a fragrance. It is stable at room temperature and soluble in many organic solvents, such as ethanol, dimethylformamide and dichloromethane.

Use:
Methyl 6-aminoindole-4 carboxylate is useful as a pharmaceutical intermediate. It has important application value in the field of biochemistry and pharmacy. For example, it can be used in the synthesis of anticancer drugs, inhibitors and modulators, etc. In addition, it can also be used in the synthesis of organic dyes and phosphors, etc.

Preparation Method:
The preparation of 6-aminoindole-4 carboxylic acid methyl ester can be carried out by the following steps:
1. Indole -4-carboxylic acid is reacted with methyl chloroformate to obtain methyl indole -4-carboxylate.
2. Indole -4-carboxylic acid methyl ester reacts with methyl chloroformate under alkaline conditions to obtain 6-amino indole -4-carboxylic acid methyl ester.

Safety Information:
Methyl 6-aminoindole-4-carboxylate is an organic compound that is generally harmful to humans and the environment. Use should comply with the relevant safety procedures. In case of skin contact, rinse with plenty of water in time. If ingested or inhaled, seek medical attention immediately. When handling or storing the compound, care should be taken to avoid reaction with strong oxidants and acids. For specific safety information, please refer to the safety data form for the compound.

Last Update：2024-04-09 20:52:54