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Benzoic acid, 2-(3-bromobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65565-11-9

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65565-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65565-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65565-11:
(7*6)+(6*5)+(5*5)+(4*6)+(3*5)+(2*1)+(1*1)=139
139 % 10 = 9
So 65565-11-9 is a valid CAS Registry Number.

65565-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-bromobenzoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-(3-bromobenzoyl)

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:65565-11-9 SDS

65565-11-9Downstream Products

65565-11-9Relevant academic research and scientific papers

Preparation and use of compounds as protease inhibitors

-

Page/Page column 26, (2008/12/07)

Disclosed are compounds of the formula I or a stereoisomer, tautomer, or pharmaceutically acceptable salt or solvate thereof, wherein Q is a bond or —N(R5)—;T is a bond, —O—, —C(O)—; S, —N(R5)—, or —C(R6′R7′);U

BROMINATION OF 2-BENZOYLBENZOIC ACIDS

Popov, S.I.,Kopylova, T.M.,Andrievskii, A.M.,Medvedev, S.V.,Yatsenko, A.V.

, p. 279 - 285 (2007/10/02)

A new method was developed for the synthesis of bromine-substituted 9,10-anthraquinones by bromination of 2-benzoylbenzoic acid derivatives in the presence of sulfuric and nitric acids followed by cyclization.

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