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Acetamide, 2-[(2-oxo-2-phenylethyl)thio]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61883-71-4

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61883-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61883-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,8 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61883-71:
(7*6)+(6*1)+(5*8)+(4*8)+(3*3)+(2*7)+(1*1)=144
144 % 10 = 4
So 61883-71-4 is a valid CAS Registry Number.

61883-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenacylsulfanyl-N-phenylacetamide

1.2 Other means of identification

Product number -
Other names S-Phenacylthioglycollanilid

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:61883-71-4 SDS

61883-71-4Relevant academic research and scientific papers

Synthesis of biologically important n-heteroaryl-2-(heteroarylthio) acetamides

Krishnaraj, Thulasiraman,Muthusubramanian, Shanmugam

, p. 1012 - 1019 (2014/08/05)

The synthesis of compounds having triazole and selena/thiadiazole rings connected by a chain having sulfur and nitrogen in the link has been described. The resultant N-heteroaryl-2-(heteroarylthio)acetamide may be biologically important as related compounds found application in the inhibition of HIV 1 replications.

A chemoselective hydroxymethylation: New route for the synthesis of 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones

Krishnaraj, Thulasiraman,Muthusubramanian, Shanmugam

experimental part, p. 1149 - 1152 (2012/03/26)

Treatment of 2-(2-oxo-2-arylethylthio)-N-(4H-1,2,4-triazol-3-yl)acetamides with paraformaldehyde in the presence of a base has led to a tandem chemoselective hydroxymethylation followed by cyclization yielding a set of novel 6-aroyl-4-(4H-triazol-3-yl)thi

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