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Phosphoric acid, 4-acetylphenyl ethyl methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

565455-55-2

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565455-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565455-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,4,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 565455-55:
(8*5)+(7*6)+(6*5)+(5*4)+(4*5)+(3*5)+(2*5)+(1*5)=182
182 % 10 = 2
So 565455-55-2 is a valid CAS Registry Number.

565455-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-acetylphenyl) ethyl methyl phosphate

1.2 Other means of identification

Product number -
Other names 4-acetylphenyl ethyl methyl phosphate

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:565455-55-2 SDS

565455-55-2Relevant academic research and scientific papers

Resolution of chiral phosphate, phosphonate, and phosphinate esters by an enantioselective enzyme library

Nowlan, Charity,Li, Yingchun,Hermann, Johannes C.,Evans, Timothy,Carpenter, Joseph,Ghanem, Eman,Shoichet, Brian K.,Raushel, Frank M.

, p. 15892 - 15902 (2007/10/03)

An array of 16 enantiomeric pairs of chiral phosphate, phosphonate, and phosphinate esters was used to establish the breadth of the stereoselective discrimination inherent within the bacterial phosphotriesterase and 15 mutant enzymes. For each substrate,

Operational control of stereoselectivity during the enzymatic hydrolysis of racemic organophosphorus compounds

Li, Yingchun,Aubert, Sarah D.,Raushel, Frank M.

, p. 7526 - 7527 (2007/10/03)

The wild-type bacterial phosphotriesterase catalyzes the stereoselective hydrolysis of racemic pairs of organophosphorus compounds. The enzymatic stereoselectivity can be substantially enhanced via systematic alteration of the pKa for the leavi

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