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Benzenamine, 4-bromo-N-[(2E)-3-phenyl-2-propenylidene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116115-79-8

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116115-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116115-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,1 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116115-79:
(8*1)+(7*1)+(6*6)+(5*1)+(4*1)+(3*5)+(2*7)+(1*9)=98
98 % 10 = 8
So 116115-79-8 is a valid CAS Registry Number.

116115-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name C6H5CHCHCHNC6H4Br-4

1.2 Other means of identification

Product number -
Other names (4-Bromo-phenyl)-[(E)-3-phenyl-prop-2-en-(E)-ylidene]-amine

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:116115-79-8 SDS

116115-79-8Relevant academic research and scientific papers

First example of the cascade acylation/IMDAV/ene reaction sequence, leading to N-arylbenzo[f]isoindole-4-carboxylic acids possessing anti-viral activity

Voronov, Alexander A.,Alekseeva, Kseniia A.,Ryzhkova, Elena A.,Zarubaev, Vladimir V.,Galochkina, Anastasia V.,Zaytsev, Vladimir P.,Majik, Mahesh S.,Tilve, Santosh G.,Gurbanov, Atash V.,Zubkov, Fedor I.

, p. 1108 - 1111 (2018)

The reaction between readily accessible N-aryl-3-phenylallylamines and maleic anhydride led to unexpected products – polysubstituted hydrogenated benzo[f]isoindole-4-carboxylic acids. This transformation proceeds through a previously unknown sequence of s

Stereoisomeric Styryl-substituted Pyrrolidines, 3,7-Diazobicyclo[3.3.0]octanes and 2-Styrylpyrroles from Cinnamaldehyde Iminium-N-methanide 1,3-Dipoles

Butler, Richard N.,Farrell, Derval M.

, p. 82 - 83 (2007/10/03)

The reaction of cinnamaldehyde N-aryliminium methanide 1,3-dipoles with dimethyl maleate, dimethyl fumarate and some N-arylmaleimides gives equal mixtures of stereoisomeric substituted pyrrolidines and a route to 2-styrylpyrroles with dimethyl acetylene-d

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