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3H-Indole-3-aceticacid(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81326-17-2

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81326-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81326-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81326-17:
(7*8)+(6*1)+(5*3)+(4*2)+(3*6)+(2*1)+(1*7)=112
112 % 10 = 2
So 81326-17-2 is a valid CAS Registry Number.

81326-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3H-indol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 3H-INDOLE-3-ACETIC 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:81326-17-2 SDS

81326-17-2Upstream product

81326-17-2Downstream Products

81326-17-2Relevant academic research and scientific papers

Enzymatic Hydrolysis of Heterocyclic Nitriles

Klempier, Norbert,Raadt, Anna de,Griengl, Herfried,Heinisch, Gottfried

, p. 93 - 95 (2007/10/02)

Chemoselective hydrolysis of heterocyclic nitriles can be achieved by an easy to use immobilized biocatalyst prepared from Rhodococcus sp.Pyrimidine-2-carbonitrile (2a) and 3-chloropyridazine-4-carbonitrile (4a) were converted into the corresponding amides while from 2-ethoxycarbonyl-4-pyridinecarbonitrile (1a), 6-methylpyridazine-3-carbonitrile (3a), 3-chloropyridazine-4-carbonitrile (4a), 3-ethoxycarbonyl-4,5-dihydroisoxazole-5-carbonitrile (8a), indole-3-carbonitrile (9a), and indole-3-ylacetonitrile (10a) the acids were formed.

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