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(E)-3-(4-(diethylamino)phenyl)acrylonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119516-35-7

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119516-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119516-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119516-35:
(8*1)+(7*1)+(6*9)+(5*5)+(4*1)+(3*6)+(2*3)+(1*5)=127
127 % 10 = 7
So 119516-35-7 is a valid CAS Registry Number.

119516-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-diethylaminocinnamonitrile

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:119516-35-7 SDS

119516-35-7Relevant academic research and scientific papers

Oxidative heck reaction as a tool for para-selective olefination of aniline: A DFT supported mechanism

Moghaddam, Firouz Matloubi,Pourkaveh, Raheleh,Karimi, Ashkan

, p. 10635 - 10640 (2018/05/31)

This study describes the first para-selective palladium-catalyzed alkenylation of tertiary amines. This regioselective C-H activation was conducted without any chelation moieties. A series of olefins were reacted under mild reaction conditions at 60 °C, and the corresponding products were obtained in good yields with high selectivity.

IMPROVED SYNTHESIS OF TRANS-4-DIETHYLAMINOCINNAMALDEHYDE

Chao, Herbert S.-I.

, p. 1641 - 1650 (2007/10/02)

The title compound was prepared from diisobutylaluminum hydride reduction of 4-diethylaminocinnamonitrile, which in turn was obtained by condensing 4-diethylaminobenzaldehyde and cyanoacetic acid.

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