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2-[(Diphenylmethyl)sulfanyl]-N-hydroxyacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63547-44-4

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63547-44-4 Usage

Derivative of N-hydroxyacetamide

Yes

Potential applications

Anticancer and antiviral agent

Additional chemical property

Presence of diphenylmethylsulfanyl group

Potential contribution

Pharmacological activity

Area of interest

Development of new therapeutic agents for various diseases and conditions

Check Digit Verification of cas no

The CAS Registry Mumber 63547-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63547-44:
(7*6)+(6*3)+(5*5)+(4*4)+(3*7)+(2*4)+(1*4)=134
134 % 10 = 4
So 63547-44-4 is a valid CAS Registry Number.

63547-44-4SDS

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-benzhydrylsulfanyl-N-hydroxyacetamide

1.2 Other means of identification

Product number -
Other names 2-[(diphenylmethyl)sulfanyl]-N-hydroxyacetamide

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:63547-44-4 SDS

63547-44-4Downstream Products

63547-44-4Relevant academic research and scientific papers

Synthesis and determination of the absolute configuration of the enantiomers of modafinil

Prisinzano, Thomas,Podobinski, John,Tidgewell, Kevin,Luo, Min,Swenson, Dale

, p. 1053 - 1058 (2004)

The asymmetric synthesis of both enantiomers of modafinil, a unique CNS stimulant with a reduced abuse liability, is described. This approach effectively prepares modafinil on a multigram scale in several steps from benzhydrol. The described synthetic route has also been used to produce the more water soluble analogue, adrafinil. X-ray crystallographic analysis on (-)-(diphenylmethanesulfinyl)acetic acid has determined the absolute configuration to be R.

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