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4-Isoxazolecarboxylic acid, 3-(4-chlorophenyl)-5-[[(phenylmethyl)amino]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

682352-98-3

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682352-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 682352-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,2,3,5 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 682352-98:
(8*6)+(7*8)+(6*2)+(5*3)+(4*5)+(3*2)+(2*9)+(1*8)=183
183 % 10 = 3
So 682352-98-3 is a valid CAS Registry Number.

682352-98-3SDS

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 5-(benzylamino-methyl)-3-(4-chloro-phenyl)-isoxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(Benzylamino-methyl)-3-(4-chloro-phenyl)-isoxazole-4-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:682352-98-3 SDS

682352-98-3Downstream Products

682352-98-3Relevant academic research and scientific papers

Insights into the bromination of 3-aryl-5-methyl-isoxazole-4-carboxylate: Synthesis of 3-aryl-5-bromomethyl-isoxazole-4-carboxylate as precursor to 3-aryl-5-formyl-isoxazole-4-carboxylate

Roy, Amrendra K.,Rajaraman,Batra, Sanjay

, p. 2301 - 2310 (2007/10/03)

Results of the detailed investigations on the bromination of the methyl group of 3-aryl-5-methyl-isoxazole-4-carboxylate, a precursor to obtain 3-aryl-5-formyl-isoxazole-4-carboxylate, are described. The products generated during the study have been utilized as substrates for the synthesis of isoxazole-fused heterocycles.

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