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919365-93-8

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919365-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 919365-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,3,6 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 919365-93:
(8*9)+(7*1)+(6*9)+(5*3)+(4*6)+(3*5)+(2*9)+(1*3)=208
208 % 10 = 8
So 919365-93-8 is a valid CAS Registry Number.

919365-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyano-N-(4-nitrophenyl)-2-(triphenyl-λ<sup>5</sup>-phosphanylidene)acetamide

1.2 Other means of identification

Product number -
Other names -

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:919365-93-8 SDS

919365-93-8Downstream Products

919365-93-8Relevant articles and documents

Synthesis, thermal reactivity, and kinetics of stabilized phosphorus ylides, part 2: [(Arylcarbamoyl) (cyano)-methylene] triphenylphos-phoranes and their thiocarbamoyl analogues

Aitken, R. Alan,Al-Awadi, Nouria A.,El-Dusouqui, Osman M.E.,Farrell, Dorcas M.M.,Kumar, Ajith

, p. 496 - 502 (2008/02/09)

A series of five cyano(arylcarbamoyl) phosphorus ylides 2 and five cyano-(arylthiocarbamoyl) phosphorus ylides 3 are prepared and fully characterized. Pyrolytic reaction products of a representative example of each type obtained by flash vacuum pyrolysis technique show that they undergo thermal extrusion of Ph3PO or Ph3PS. Kinetic study of the gas-phase pyrolysis of each ylide by static method shows that these reactions are unimolecular and first order with no significant substituent effect, but the thiocarbamoyl ylides 3 react 40-65 times more rapidly than their carbamoyl analogues 2.

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