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4-(4-bromobenzoyl)-4-(2-cyanoethyl)heptanedinitrile is a complex organic compound with the molecular formula C18H18BrN3O2. It features a heptanedinitrile backbone, which consists of a seven-carbon chain with two nitrile (CN) groups. The compound is further characterized by a 4-bromobenzoyl group attached to the fourth carbon, which is a benzoyl group (a benzene ring with a carbonyl group) substituted with a bromine atom. Additionally, a 2-cyanoethyl group is attached to the same carbon, which is an ethyl group (two carbons) with a cyano group (CN). This molecule is likely to be used in the synthesis of more complex organic compounds or as an intermediate in chemical reactions due to its diverse functional groups.

6328-38-7

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6328-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6328-38-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6328-38:
(6*6)+(5*3)+(4*2)+(3*8)+(2*3)+(1*8)=97
97 % 10 = 7
So 6328-38-7 is a valid CAS Registry Number.

6328-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-bromobenzoyl)-4-(2-cyanoethyl)heptanedinitrile

1.2 Other means of identification

Product number -
Other names 4-(4-bromo-benzoyl)-4-(2-cyano-ethyl)-heptanedinitrile

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:6328-38-7 SDS

6328-38-7Downstream Products

6328-38-7Relevant academic research and scientific papers

Enviornmentally benign michael and claisen schmidt reaction of aromatic carbonyl compounds by alkaline polyionic resin

Jaitak, Vikas,Kaul,Das, Pralay

, p. 1137 - 1145 (2013/09/24)

A regioselective Michael reaction between aryl methyl ketones and α,β-unsaturated compounds has been carried out using basic polyionic resin as a reusable reagent. Results indicate that the reaction proceeds in consecutive manner as double Michael (27-65%) and triple Michael (40-45%) products with overall yields of 55-80%. Moreover, A-2XMP resin has also been applied on Claisen Schmidt condensations of aromatic aldehydes and ketones (acyclic as well as cyclic) under different reaction conditions yielding dehydrated products in 82-94% yield. The reactions give an opportunity for easy separation, reusability of polyionic resin and easy purification of products in continuous or multiple processing of organic compounds.

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