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CAS

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187607-71-2

4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER is a chemical compound with the molecular formula C13H15NO4, derived from the natural compound indole found in various plants and fungi. It is a methyl ester derivative with potential pharmaceutical applications, particularly in the development of new drugs. 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER has been researched for its potential anti-inflammatory, anti-cancer, and anti-viral properties, as well as its ability to inhibit 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.

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  • 187607-71-2 Structure

  • Basic information

    1. Product Name: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER
    2. Synonyms: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER;AKOS JY2083576;METHYL 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLATE
    3. CAS NO:187607-71-2
    4. Molecular Formula: C12H13NO4
    5. Molecular Weight: 235.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 187607-71-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(187607-71-2)
    11. EPA Substance Registry System: 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER(187607-71-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 187607-71-2(Hazardous Substances Data)

187607-71-2 Usage

Uses

Used in Pharmaceutical Industry:
4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER is used as a potential drug candidate for the development of new medications due to its potential anti-inflammatory, anti-cancer, and anti-viral properties.
Used in Antimicrobial Applications:
In the field of microbiology, 4,7-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER is used as an antimicrobial agent for inhibiting the growth of certain bacteria and fungi, showcasing its potential in combating infections and diseases caused by these microorganisms.

Check Digit Verification of cas no

The CAS Registry Mumber 187607-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,6,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 187607-71:
(8*1)+(7*8)+(6*7)+(5*6)+(4*0)+(3*7)+(2*7)+(1*1)=172
172 % 10 = 2
So 187607-71-2 is a valid CAS Registry Number.

187607-71-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4,7-dimethoxy-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 4,7-dimethoxyindole-2-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:187607-71-2 SDS

187607-71-2Upstream product

187607-71-2Downstream Products

187607-71-2Relevant articles and documents

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

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Paragraph 0057-0062, (2020/06/02)

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.

Synthesis of symmetrical and unsymmetrical diindolylmethanes via acid-catalysed electrophilic substitution reactions

Bingul, Murat,Cheung, Belamy B.,Kumar, Naresh,Black, David StC.

, p. 7363 - 7369 (2017/09/12)

A range of activated indole-2-carboxylate derivatives was prepared via the Hemetsberger indole synthesis. Vilsmeier formylation was explored to establish regioselectivity and to prepare a range of new indole carbaldehydes. The indole aldehydes were reduce

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

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, (2008/06/13)

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

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