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Benzenepropanenitrile, b-(diphenylphosphinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57519-81-0

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57519-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57519-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57519-81:
(7*5)+(6*7)+(5*5)+(4*1)+(3*9)+(2*8)+(1*1)=150
150 % 10 = 0
So 57519-81-0 is a valid CAS Registry Number.

57519-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-(diphenylphosphoryl)-3-phenylpropanenitrile)

1.2 Other means of identification

Product number -
Other names 3-(diphenylphosphoryl)-3-phenylpropanenitrile

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:57519-81-0 SDS

57519-81-0Downstream Products

57519-81-0Relevant academic research and scientific papers

P-C Bond formation via direct and three-component conjugate addition catalyzed by 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD)

Jiang, Zhiyong,Zhang, Yan,Ye, Weiping,Tan, Choon-Hong

, p. 51 - 54 (2007)

The direct addition of P(O)-H bonds (dialkyl phosphites and diphenyl phosphonite) across various activated alkenes was catalyzed effectively by 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD). This is a mild, rapid and efficient protocol to generate P-C bonds.

Bronsted acid mediated nitrogenation of propargylic alcohols: An efficient approach to alkenyl nitriles

Huang, Xiaoqiang,Jiao, Ning

supporting information, p. 4324 - 4328 (2014/06/23)

A novel and efficient approach to alkenyl nitriles from readily available propargylic alcohols has been developed. This nitrogenation reaction is transition-metal-free and could be conducted under air at ambient temperature, which makes this protocol promising and practical. Moreover, NH4Br is disclosed as an efficient additive to promote the stereoselectivity of this reaction. the Partner Organisations 2014.

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