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6976-59-6

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6976-59-6 Usage

General Description

4-bromophenyl 4-bromooctanoate is a chemical compound that belongs to the class of organic compounds known as aryl-alkyl ketones. It is a synthetic ester formed by the reaction of 4-bromophenyl and 4-bromooctanoic acid. 4-bromophenyl 4-bromooctanoate is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has potential applications in the field of organic chemistry and material science. The presence of bromine atoms in the compound adds to its reactivity and versatility, making it a valuable building block for the synthesis of various chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 6976-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6976-59:
(6*6)+(5*9)+(4*7)+(3*6)+(2*5)+(1*9)=146
146 % 10 = 6
So 6976-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H19BrO2/c1-2-3-4-5-6-7-14(16)17-13-10-8-12(15)9-11-13/h8-11H,2-7H2,1H3

6976-59-6SDS

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-bromophenyl 4-bromooctanoate

1.2 Other means of identification

Product number -
Other names Octanoic acid 4-bromophenyl ester

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:6976-59-6 SDS

6976-59-6Relevant articles and documents

Visible-Light-Driven Dehydrogenative Coupling of Primary Alcohols with Phenols Forming Aryl Carboxylates

Ishida, Naoki,Kawasaki, Tairin,Murakami, Masahiro,Tosaki, Tomohiro

supporting information, p. 7683 - 7687 (2021/10/12)

A preparative method for obtaining aryl esters from aliphatic primary alcohols and phenols was developed. The reaction proceeds under the irradiation of visible light at ambient temperature, dispensing with any oxidant or hydrogen acceptor. Primary alcohols having a variety of functional groups are successfully esterified with phenols. The produced esters can be utilized as the precursor of various carbonyl compounds.

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