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2-(2-amino-4-chloro-3-methoxyphenyl)-4,4-dimethyl-2-oxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129634-23-7

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129634-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129634-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,3 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 129634-23:
(8*1)+(7*2)+(6*9)+(5*6)+(4*3)+(3*4)+(2*2)+(1*3)=137
137 % 10 = 7
So 129634-23-7 is a valid CAS Registry Number.

129634-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-amino-4-chloro-3-methoxyphenyl)-4,4-dimethyl-2-oxazoline

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:129634-23-7 SDS

129634-23-7Relevant academic research and scientific papers

Regioselective synthesis of 4-chloro-3-hydroxyanthranilic acid, a potent in vitro inhibitor of 3-hydroxyanthranilic acid oxygenase activity from rat brain

Melikian,Boigegrain,Kan,Soubrie

, p. 267 - 270 (2007/10/02)

In the kynurenine metabolic pathways of tryptophan in kidney, liver and brain, 3-hydroxyanthranilic oxygenase (3-HAO, EC 1.13.11.6) catalyses the conversion of 3-hydroxyanthranilic acid to quinolinic acid, an excitatory amino acid putatively involved in brain neurodegenerative disorders. The compound 4-chloro-3-hydroxyanthranilic acid is an irreversible inhibitor of 3-HAO in the liver and the kidney. We describe here a new, unambiguous regioselective synthesis of this inhibitor and verify its activity on 3-HAO at the brain level.

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