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5344-75-2

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5344-75-2 Usage

Type of compound

sulfanylacetamide derivative

Potential therapeutic properties

under investigation

Studied for potential as a drug

for the treatment of various conditions (requires further research)

Chemical structure contains

a benzothiazole ring, an ethoxy group, and a methylphenyl group

Value in medicinal chemistry research

considered valuable

Check Digit Verification of cas no

The CAS Registry Mumber 5344-75-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5344-75:
(6*5)+(5*3)+(4*4)+(3*4)+(2*7)+(1*5)=92
92 % 10 = 2
So 5344-75-2 is a valid CAS Registry Number.

5344-75-2SDS

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 1,2-DIPHENYLGLYOXAL, O-BENZYLOXIME

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:5344-75-2 SDS

5344-75-2Downstream Products

5344-75-2Relevant articles and documents

Reactions of α-Hydroxy Carbonyl Compounds with Azodicarboxylates and Triphenylphosphine: Synthesis of α-N-Hydroxy Amino Acid Derivatives

Kolasa, Teodozyj,Miller, Marvin J.

, p. 4978 - 4984 (2007/10/02)

Reaction of aliphatic α-hydroxy esters with azodicarboxylates and triphenylphosphine in the presence of either CbzNHOCH2Ph or trOCNHOCH2Ph provides a direct route to protected α-N-hydroxy amino acids.Similar reactions with aromatic α-hydroxy carbonyl compounds and derivatives result in predominate oxidation to the corresponding α-oxo carbonyl derivatives.

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