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1-Propanamine, N-(triphenylphosphoranylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67277-90-1

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67277-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67277-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,7 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67277-90:
(7*6)+(6*7)+(5*2)+(4*7)+(3*7)+(2*9)+(1*0)=161
161 % 10 = 1
So 67277-90-1 is a valid CAS Registry Number.

67277-90-1SDS

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 triphenyl(propylimino)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Propylimino-triphenyl-phosphin

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:67277-90-1 SDS

67277-90-1Relevant academic research and scientific papers

PHOSPHONIUM DIAZA-DIYLIDS AND AZA-YLDIID AS NEW AND EFFICIENT REAGENTS FOR PRIMARY AND SECONDARY AMINES SYNTHESIS

Cristau, Henri-Jean,Garcia, Chantal,Kadoura, Jumah,Torreilles, Eliane

, p. 151 - 154 (2007/10/02)

Metallated aminophosphonium ylids, diaza-diylids and aza-yldiid, are investigated as reagents for primary and secondary amines synthesis.

Alkylation et acylation de la triphenylphosphinimine N-lithiee

Cristau, Henri-Jean,Kadoura, Jumaah,Chiche, Laurent,Torreilles, Eliane

, p. 515 - 520 (2007/10/02)

A new synthetic approach to primary and secondary amines using N-lithiated triphenylphosphinimine is reported.This key reagent, accessible in two steps from dibromortiphenylphosphorane and ammonia, when treated with electrophiles yields N-substituted triphenylphosphinimine derivatives.These can react to give N-mono or disubstituted triphenylphosphonium salts which upon hydrolysis lead to the corresponding primary and secondary amines.

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