METHYL 5-METHOXY-1H-INDOLE-3-CARBOXYLATE

METHYL 5-METHOXY-1H-INDOLE-3-CARBOXYLATE - Names and Identifiers

Name	5-Methoxy-1H-indole-3-carboxylicacidmethyl ester
Synonyms	RARECHEM AL BF 0096 Methyl 5-Methoxy-indole-3-carboxylate METHYL 5-METHOXY-1H-INDOLE-3-CARBOXYLATE Methyl 5-methoxy-1H-indole-3-carboxylate methyl 5-methoxy-1H-indole-3-carboxylic acid 5-Methoxy-1H-indole-3-carboxylicacidmethyl ester 5-METHOXY-1H-INDOLE-3-CARBOXYLIC ACID METHYL ESTER 5-Methoxyl-1H-3-Indole-carboxylicacid,, Methyl ester 1H-Indole-3-carboxylic acid, 5-methoxy-, methyl ester
CAS	172595-68-5

METHYL 5-METHOXY-1H-INDOLE-3-CARBOXYLATE - Physico-chemical Properties

Molecular Formula	C11H11NO3
Molar Mass	205.21
Boling Point	370.062℃ at 760 mmHg
Appearance	Ash powder
Storage Condition	Sealed in dry,Room Temperature

METHYL 5-METHOXY-1H-INDOLE-3-CARBOXYLATE - Introduction

It is an organic compound with the chemical formula C12H11NO3.

Nature:
-Appearance: Colorless to light yellow crystal
-Melting point: about 107-110 ° C
-Solubility: Soluble in organic solvents such as methanol, dichloromethane and dimethyl sulfoxide

Use:
E-ster is commonly used in organic synthesis research and drug discovery. As an intermediate, it can be used in the synthesis of other organic compounds and drugs, such as indole antitumor drugs, indole alkaloids and so on.

Method:
The preparation of e-ster can usually be carried out through the following steps:
1. Reacting 5-methoxy -1H-indole with formic acid to obtain 5-methoxy -1H-indole -3-carboxylic acid;
2. React 5-methoxy-1H-indole-3-carboxylic acid with methanol to generate Erster.

Safety Information:
There is limited information on the safety of e-ster, but in general, you should use caution and follow relevant safety procedures for any chemical substance. It may be irritating and toxic, so it is necessary to take appropriate protective measures during operation, such as wearing protective glasses, gloves and laboratory coats, and ensure that the operating environment is well ventilated. During use or storage, care should be taken to avoid contact with oxidants, strong acids or strong bases to avoid unsafe chemical reactions.

Last Update：2024-04-09 20:49:11