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46207-73-2

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46207-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46207-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,2,0 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 46207-73:
(7*4)+(6*6)+(5*2)+(4*0)+(3*7)+(2*7)+(1*3)=112
112 % 10 = 2
So 46207-73-2 is a valid CAS Registry Number.

46207-73-2SDS

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 ethyl phenyl hydrogen phosphate

1.2 Other means of identification

Product number -
Other names Aethyl-phenyl-hydrogenphosphat

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:46207-73-2 SDS

46207-73-2Relevant articles and documents

METAL-FREE DIRECT ARYLATION OF DIALKYL PHOSPHONATES FOR THE SYNTHESIS OF MIXED ALKYL ARYL PHOSPHONATES

-

Paragraph 00449, (2019/02/15)

Provided herein are phosphates, thiophosphates, phosphonates, and phosphinates, methods of making same, and methods of using these compounds and methods for the generation of pharmaceutically relevant phosphate, phosphonate, and phosphinate analogs. This

Substrate and stereochemical specificity of the organophosphorus acid anhydrolase from Alteromonas sp. JD6.5 toward p-nitrophenyl phosphotriesters

Hill, Craig M.,Wu, Feiyue,Cheng, Tu-Chen,Defrank, Joseph J.,Raushel, Frank M.

, p. 1285 - 1288 (2007/10/03)

The enzyme OPAA hydrolyzes p-nitrophenyl phosphotriesters bearing substituents at the phosphorus center ranging in size from methyl to phenyl. The enzyme exhibits stereoselectivity toward the hydrolysis of chiral substrates with a preference for the S(P)

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