187607-71-2

Basic information

• Product Name: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER
• Synonyms: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER;AKOS JY2083576;METHYL 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLATE
• CAS NO: 187607-71-2
• Molecular Formula: C12H13NO4
• Molecular Weight: 235.24
• Mol File: 187607-71-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(187607-71-2)
• EPA Substance Registry System: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(187607-71-2)

Safety Data

• Hazardous Substances Data: 187607-71-2(Hazardous Substances Data)

Usage

General Description

4,7-Dimethoxy-1H-indole-2-carboxylic acid methyl ester is a chemical compound with the molecular formula C13H15NO4. It is derived from the natural compound indole, which is found in various plants and fungi. This particular methyl ester derivative has potential pharmaceutical applications, particularly in the development of new drugs. It has been researched for its potential anti-inflammatory, anti-cancer, and anti-viral properties. Additionally, it has shown promise in inhibiting the growth of certain bacteria and fungi. Overall, 4,7-Dimethoxy-1H-indole-2-carboxylic acid methyl ester is a compound with diverse potential biological and pharmaceutical applications.

Upstream product

• 93-02-7 2,5-dimethoxybenzaldehyde 

Relevant articles and documents

Preparation method of methoxy-substituted methyl-1H-indole-2-carboxylate

The invention relates to the technical field of organic synthesis, and provides a preparation method of methoxy-substituted methyl-1H-indole-2-carboxylate. The preparation method comprises the following steps: mixing methoxy-substituted methyl(Z)-2-azido-3-phenyl acrylate, a ruthenium catalyst and tetrahydrofuran, and carrying out a cyclization reaction to obtain the methoxy-substituted methyl-1H-indole-2-carboxylate. According to the preparation method provided by the invention, the ruthenium catalyst is adopted for catalysis, and the methoxy-substituted methyl-1H-indole-2-carboxylate can beprepared without using high-toxicity toluene and high-toxicity xylene as solvents. The preparation method provided by the invention is relatively low in toxicity and relatively high in safety coefficient; and the yield of a product, namely the methoxy-substituted methyl-1H-indole-2-carboxylate purified by the method provided by the invention is relatively high and is 93% or above.

Indole-2-carboxylate derivatives and fungicidal compositions for agricultural or horticultural use containing the derivatives as active component

An object of the invention is to provide an indole-2-carboxylic acid ester derivative which shows a selectively high fungicidal effect on fungicide-resistant fungi. The indole-2-carboxylic acid ester derivative of the invention is a compound represented b