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7077-62-5

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7077-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7077-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7077-62:
(6*7)+(5*0)+(4*7)+(3*7)+(2*6)+(1*2)=105
105 % 10 = 5
So 7077-62-5 is a valid CAS Registry Number.

7077-62-5SDS

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 trimethyl-N-phenyl-phosphorimidate

1.2 Other means of identification

Product number -
Other names N-Phenyl-trimethoxy-phosphinimin

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:7077-62-5 SDS

7077-62-5Relevant articles and documents

Reactions de tris(alcoxy)iminophosphanes avec l'acetylene dicarboxylate de methyle: ylure, phosphonate et phosphorane

Bellan, Jacques,Sanchez, Michel,Marre-Mazieres, Marie-Rose,Murillo Beltran, Arturo

, p. 491 - 495 (2007/10/02)

The tris(alkoxy) N-phenyl iminophosphanes react under mild conditions with acetylenic carboxylates to give phosphorus ylides with a β carbonyl group.These compounds, well characterized in the reaction mixture, have not been isolated.They are highly reactive and depending on the nature of substituents on phosphorus atom; give phosphonates, phosphoranes and cyclic ylides.

INDUCTIVE AND STERIC EFFECTS IN THE STAUDINGER REACTION

Gololobov, Yu.,Kasukhin, L.,Ponomarchuk, M.,Klepa, T.,Yurchenko, R.

, p. 339 - 342 (2007/10/02)

The sterically unhindered mode of the electrophilic addition of phenyl azide to trivalent phosphorus compounds and the inductive control in this initial step of the Staudinger reaction have been observed and discussed.

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