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103871-31-4

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103871-31-4 Usage

Structure

A chemical compound that is a phenylmethyl ester derivative of 1H-indole-1-carboxylic acid, containing a hydroxyethyl group.

Biological and pharmacological activities

The compound has potential biological and pharmacological activities, with studies indicating its potential use in the development of pharmaceutical drugs.

Research and development

It is commonly used in research and development to study its effects and potential applications in various fields, particularly in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 103871-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,7 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103871-31:
(8*1)+(7*0)+(6*3)+(5*8)+(4*7)+(3*1)+(2*3)+(1*1)=104
104 % 10 = 4
So 103871-31-4 is a valid CAS Registry Number.

103871-31-4SDS

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 benzyl 3-(1-hydroxyethyl)indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:103871-31-4 SDS

103871-31-4Relevant articles and documents

Structure-activity dependency of new bacterial tryptophanyl tRNA synthetase inhibitors

Witty, David R.,Walker, Graham,Bateson, John H.,O'Hanlon, Peter J.,Cassels, Robert

, p. 1375 - 1380 (2007/10/03)

Analogues of the aminoacyl tRNA synthetase inhibitor, indolmycin, have been synthesised in which the side chain methyl group is replaced by a wide range of substituents. Their antibacterial and enzyme inhibitory potency is related to steric properties and

Antibacterial 2-amino-oxazolinones and process therefor

-

, (2008/06/13)

A series of novel antibacterially active derivatives of indolmycin as well as some prodrug forms of indolmycin is disclosed. A novel process for the production of these compounds is also disclosed.

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