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86012-83-1

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86012-83-1 Usage

General Description

4,6-Indole dicarboxylic acid methyl ester is a chemical compound that consists of an indole core with two carboxylic acid functional groups and a methyl ester substituent. It is commonly used in organic synthesis and pharmaceutical research due to its potential as a building block for the construction of various biologically active compounds. The compound has been found to exhibit antioxidant and anti-inflammatory properties, making it a promising candidate for drug development. Its structure and chemical properties make it a versatile ingredient in the development of new pharmaceutical drugs and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 86012-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,1 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86012-83:
(7*8)+(6*6)+(5*0)+(4*1)+(3*2)+(2*8)+(1*3)=121
121 % 10 = 1
So 86012-83-1 is a valid CAS Registry Number.

86012-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxycarbonyl-1H-indole-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-(methoxycarbonyl)-1H-indole-6-carboxylic acid

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:86012-83-1 SDS

86012-83-1Downstream Products

86012-83-1Relevant articles and documents

Diels-Alder Reactions of Vinyl Derivatives of Five-Membered Monoheterocyclic Compounds

Noland, Wayland E.,Lee, Chang Kiu,Bae, Sun Kun,Chung, Bong Yul,Hahn, Chi Sun,Kim, Keun Jae

, p. 2488 - 2491 (1983)

Vinylpyrroles having electron-withdrawing substituents react with dienophiles to give ? adducts while the furan and thiophene analogues do not.The difference in reactivity among the monoheterocycles can be explained in terms of the greater electron-releasing ability of the nitrogen atom in the pyrrole.The s-cis conformation of the (1H-pyrrol-2-yl)maleate derivatives appears to be an important factor in their undergoing the cycloaddition reaction.

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