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56961-27-4

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56961-27-4 Usage

Chemical Properties

off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 56961-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,6 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56961-27:
(7*5)+(6*6)+(5*9)+(4*6)+(3*1)+(2*2)+(1*7)=154
154 % 10 = 4
So 56961-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrClO2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3H,(H,10,11)

56961-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-2-chlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-bromo-2-chloro-benzoic acid

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:56961-27-4 SDS

56961-27-4Relevant articles and documents

Design, synthesis, and structure-activity relationship of a novel series of 2-aryl 5-(4-oxo-3-phenethyl-2-thioxothiazolidinylidenemethyl)furans as HIV-1 entry inhibitors

Katritzky, Alan R.,Tala, Srinivasa R.,Lu, Hong,Vakulenko, Anatoliy V.,Chen, Qi-Yin,Sivapackiam, Jothilingam,Pandya, Keyur,Jiang, Shibo,Debnath, Asim K.

supporting information; experimental part, p. 7631 - 7639 (2010/09/03)

We previously identified two small molecules targeting the HIV-1 gp41, N-(4-carboxy-3-hydroxy)phenyl-2,5-dimethylpyrrole 12 (NB-2) and N-(3-carboxy-4-chloro)phenylpyrrole 13 (NB-64), that inhibit HIV-1 infection at low micromolar levels. On the basis of m

Ortho-metalation of unprotected 3-bromo and 3-chlorobenzoic acids with hindered lithium dialkylamides

Gohier, Frederic,Mortier, Jacques

, p. 2030 - 2033 (2007/10/03)

Upon treatment of 3-chloro/bromobenzoic acids with hindered lithium dialkylamides (LDA or LTMP) at -50 °C, lithium 3-chloro/bromo-2-lithiobenzoates are generated. These dianions can be trapped as such to afford after electrophilic quenching a variety of s

Lithiations directed by carboxylic acid, fluorine and chlorine: The regioselective synthesis of polysubstituted benzoic acids and acetophenones

Moyroud, Joel,Guesnet, Jean-Luc,Bennetau, Bernard,Mortier, Jacques

, p. 133 - 141 (2007/10/03)

Lithiation/electrophilic quenching of ortho-lithiated benzoates allows the totally regiocontrolled synthesis of a wide range of 2,3-, 2,3,4-, and 2,3,4,5-polysubstituted benzoic acids and related acetophenones. Elsevier,.

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