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2-Propenenitrile, 3-amino-3-(3-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27545-73-9

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27545-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27545-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27545-73:
(7*2)+(6*7)+(5*5)+(4*4)+(3*5)+(2*7)+(1*3)=129
129 % 10 = 9
So 27545-73-9 is a valid CAS Registry Number.

27545-73-9SDS

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 3-amino-3-(3-chlorophenyl)prop-2-enenitrile

1.2 Other means of identification

Product number -
Other names 3-(m-Chlor-phenyl)-3-amino-acrylonitril

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:27545-73-9 SDS

27545-73-9Relevant academic research and scientific papers

ROCK-INHIBITING COMPOUND AND USES THEREOF

-

Paragraph 0089; 0090, (2020/05/07)

Disclosed herein are a compound of formula (I) and a preparation method and uses thereof. The compound shows a good inhibitory activity against ROCK, providing a new medicinal strategy to clinically treat the diseases associated with abnormal ROCK activity.

Acid-promoted rapid solvent-free access to substituted 1,4-dihydropyridines from β-ketothioamides

Li, Ming,Sun, Ke-Na,Wen, Li-Rong

, p. 21535 - 21539 (2016/03/08)

β-Ketothioamides (KTAs) have been used as building blocks with aldehydes and β-enaminonitriles for synthesis of 1,4-dihydropyridines in the presence of AcOH under solvent-free conditions within 5 min. This new strategy exhibits remarkable features such as high chemoselectivity, mild reaction conditions, easily available substrates, and good yields.

Rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles

Ma, Miaofeng,Hou, Guohua,Wang, Junru,Zhang, Xumu

experimental part, p. 506 - 511 (2011/06/17)

The rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles was investigated by using monophosphine and bisphosphine ligands. It was found that an Rh-QuinoxP complex exhibited high enantioselectivities for β-aryl substituted β-acetylamino acrylonitriles and the Rh-JosiPhos CyPF-t-Bu complex was proven to be effective for the hydrogenation of tetrasubstituted olefins from cyclic β-acetylamino acrylonitriles.

Highly efficient RhI-catalyzed asymmetric hydrogenation of β-amino acrylonitriles

Ma, Miaofeng,Hou, Guohua,Sun, Tian,Zhang, Xiaowei,Li, Wei,Wang, Junru,Zhang, Xumu

supporting information; experimental part, p. 5301 - 5304 (2010/09/08)

(Figure Presented) It takes two to TangPhos: β-Amino acrylonitriles can be readily prepared from acetonitriles. Both of the E/Z isomers undergo hydrogenation with excellent enantioselectivity by using the Rh-TangPhos (TangPhos = l, 1'-ditert-butyl-(2, 2')-diphospholane) catalyst system. The products, chiral β-amino nitriles, are valuable chiral building blocks for many drugs.

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