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14370-71-9

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14370-71-9 Usage

General Description

(2-hydroxy-1H-indol-3-yl)(oxo)acetic acid is a chemical compound with the molecular formula C10H7NO4. It is a derivative of indole, a bicyclic heterocyclic organic compound. The presence of a hydroxyl group and a carbonyl group in its structure makes it a functional organic molecule with potential biological activity. It may have applications in the pharmaceutical industry, particularly in the development of new drugs or as a key intermediate in the synthesis of other organic compounds. The compound's structure suggests that it may have potential therapeutic uses, and further research may elucidate its role in various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 14370-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14370-71:
(7*1)+(6*4)+(5*3)+(4*7)+(3*0)+(2*7)+(1*1)=89
89 % 10 = 9
So 14370-71-9 is a valid CAS Registry Number.

14370-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-2-(2-oxo-1H-indol-3-ylidene)acetic acid

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

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More Details:14370-71-9 SDS

14370-71-9Downstream Products

14370-71-9Relevant articles and documents

Preparation of 7-Hydroxy-2-oxoindolin-3-ylacetic Acid and its , -(3)H>, and -7-O-Glucosyl Analogues for Use in the Study of Indol-3-yl-acetic Acid Catabolism

Lewer, Paul

, p. 753 - 758 (2007/10/02)

An improved synthesis of 7-hydroxy-2-oxoindolin-3-ylacetic acid (14) via the base-induced condensation reaction between oxalate esters and 7-benzyloxyindolin-2-one is described. 7-Benzyloxyindolin-2-one was prepared in four steps and 50percent overall yie

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