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2-Propanone, 1-(2-chlorophenyl)-1-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64543-64-2

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64543-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64543-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64543-64:
(7*6)+(6*4)+(5*5)+(4*4)+(3*3)+(2*6)+(1*4)=132
132 % 10 = 2
So 64543-64-2 is a valid CAS Registry Number.

64543-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloro-phenyl)-1-hydroxy-acetone

1.2 Other means of identification

Product number -
Other names 1-(2-Chlor-phenyl)-1-hydroxy-aceton

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:64543-64-2 SDS

64543-64-2Relevant academic research and scientific papers

Catalytic scope of the thiamine-dependent multifunctional enzyme cyclohexane-1,2-dione hydrolase

Loschonsky, Sabrina,Waltzer, Simon,Fraas, Sonja,Wacker, Tobias,Andrade, Susana L. A.,Kroneck, Peter M. H.,Mueller, Michael

, p. 389 - 392 (2014/03/21)

The thiamine diphosphate (ThDP)-dependent enzyme cyclohexane-1,2-dione hydrolase (CDH) was expressed in Escherichia coli and purified by affinity chromatography (Ni-NTA). Recombinant CDH showed the same Ci￡C bond-cleavage and Ci￡C bond-formation activitie

Nucleophilic acylation of esters by acid chlorides mediated by samarium diiodide: Formation and use of samarium enediolates.

Machrouhi, Fouzia,Namy, Jean-Louis,Kagan, Henri B.

, p. 7183 - 7186 (2007/10/03)

Acid chlorides react with esters in the presence of samarium diiodide and catalytic amounts of NiI2 to afford samarium enediolates which can further react with electrophiles such as water or aldehydes to give respectively α-ketols or α-dihydroxyketones.

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