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Benzenepropanethioic acid, b-hydroxy-, S-(4-chlorophenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62547-65-3

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62547-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62547-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62547-65:
(7*6)+(6*2)+(5*5)+(4*4)+(3*7)+(2*6)+(1*5)=133
133 % 10 = 3
So 62547-65-3 is a valid CAS Registry Number.

62547-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-S-(4-Chlorophenyl) 3-hydroxy-3-phenylpropanethioate

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-3-phenyl-thiopropionic acid S-(4-chloro-phenyl) ester

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:62547-65-3 SDS

62547-65-3Downstream Products

62547-65-3Relevant academic research and scientific papers

Bioinspired, base- and metal-free, mild decarboxylative aldol activation of malonic acid half thioesters under phase-transfer reaction conditions

Bew, Sean P.,Stephenson, G. Richard,Rouden, Jacques,Ashford, Polly-Anna,Bourane, Manuel,Charvet, Agathe,Dalstein, Virginie M. D.,Jauseau, Raphael,Hiatt-Gipson,Martinez-Lozano, Luis A.

, p. 1245 - 1257 (2015/04/22)

Utilizing 'off the shelf' commercially available, cheap, small synthetic molecules that mimic the efficient mediation of important bioreactions utilized by Nature is not only highly sought after but also currently highly topical. This paper details our preliminary efforts at developing a unique base- and metal-free phase-transfer-mediated malonic acid thioester (MAHT) 'activation protocol' that efficiently generates (±)-β-thioesters. Our bioinspired aldol process is exceptionally mild, conducted under near neutral pH reaction conditions, does not require an inert, oxygen-free atmosphere or anhydrous reaction conditions and is highly atom-economic. Exemplifying the utility of our protocol, the synthesis of an array of structurally and functionally diverse (±)-β-hydroxy thioesters equipped with highly prized functionality, i.e., chlorine, bromine, fluorine, nitrile and nitro groups, is reported, as is the diastereoselective potential of this important reaction.

S-(4-chlorophenyl) 3-aryl-3-hydroxypropanethioates as antibacterial agents

Snyder Jr.,Burrous,Freedman,Herbert

, p. 413 - 415 (2007/10/15)

A series of S-(4-chlorophenyl) 3-aryl-3-hydroxypropanethioates was prepared and shown to have in vitro activity against several selected bacterial species.

S-(4-Chlorophenyl)-3-aryl-3-hydroxypropanethioates

-

, (2008/06/13)

A series of S-(4-Chlorophenyl)-3-aryl-3-hydroxypropanethioates are effective as antibacterial agents.

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