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470716-52-0

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470716-52-0 Usage

General Description

The chemical compound "(4-chlorophenyl)(2,5-difluorobenzyl)sulfane" is a sulfane compound with a 4-chlorophenyl group bonded to a (2,5-difluorobenzyl) group. Sulfane compounds are sulfur analogs of organic peroxides and are known for their potential biological and pharmaceutical applications. This specific compound may have potential uses in pharmaceutical development or as a chemical intermediate in organic synthesis. Its unique structure and potential reactivity make it a subject of interest for further research in the fields of chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 470716-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,7,1 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 470716-52:
(8*4)+(7*7)+(6*0)+(5*7)+(4*1)+(3*6)+(2*5)+(1*2)=150
150 % 10 = 0
So 470716-52-0 is a valid CAS Registry Number.

470716-52-0SDS

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 2-{[(4-Chlorophenyl)sulfanyl]methyl}-1,4-difluorobenzene

1.2 Other means of identification

Product number -
Other names 2-(4-Chlor-phenylmercapto)-1-phenyl-aethanon

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:470716-52-0 SDS

470716-52-0Relevant articles and documents

A practical synthesis of a γ-secretase inhibitor

Scott, Jeremy P.,Lieberman, David R.,Beureux, Olivier M.,Brands, Karel M. J.,Davies, Antony J.,Gibson, Andrew W.,Hammond, Deborah C.,McWilliams, Chris J.,Stewart, Gavin W.,Wilson, Robert D.,Dolling, Ulf-H.

, p. 4149 - 4155 (2008/02/05)

(Chemical Equation Presented) A practical and scaleable synthesis of the γ-secretase inhibitor 1 is reported. The inhibitor consists of a central trisubstituted cyclohexane core with appended propionic acid, 2,5-difluorophenyl, and 4-chlorophenylsulfonyl

HETEROCYCLIC METHYL SULFONE DERIVATIVE

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Page/Page column 16, (2010/11/08)

Provided is a compound capable of inhibiting production or secretion of β amyloid protein. A compound represented by the following formula (1): (wherein, R1 represents a heterocyclic group which may have a substituent, R2 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R3 represents a cyclic hydrocarbon group which may have a substituent or a heterocyclic group which may have a substituent, R4 represents a hydrogen atom or a C1-6 alkyl group, and X represents -S-,-SO- or -SO2-) an N-oxide or S-oxide thereof; a salt thereof; or a solvate thereof; and a medicament containing any of them.

The new cyclohexylpropionic sulfone

-

Page/Page column 12, (2008/06/13)

Novel sulphones of formula I are disclosed: The compounds modulate the processing of amyloid precursor protein by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.

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