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16588-24-2

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16588-24-2 Usage

General Description

5-Bromo-2-chloronitrobenzene is a chemical compound with the molecular formula C6H3BrClNO2. It is a derivative of nitrobenzene with a bromine and chlorine substituent. 5-BROMO-2-CHLORONITROBENZENE is a yellow solid that is sparingly soluble in water but soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. 5-Bromo-2-chloronitrobenzene is also used as a building block in the production of other chemicals and is handled and stored with care due to its potential hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 16588-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16588-24:
(7*1)+(6*6)+(5*5)+(4*8)+(3*8)+(2*2)+(1*4)=132
132 % 10 = 2
So 16588-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrClNO2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H

16588-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-1-chloro-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 5-Bromo-2-chloronitrobenzene

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:16588-24-2 SDS

16588-24-2Relevant articles and documents

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Hammond,Modic

, p. 1385 (1953)

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Pd-Catalyzed Decarboxylative Ortho-Halogenation of Aryl Carboxylic Acids with Sodium Halide NaX Using Carboxyl as a Traceless Directing Group

Fu, Zhengjiang,Jiang, Yongqing,Wang, Shuiliang,Song, Yuanyuan,Guo, Shengmei,Cai, Hu

supporting information, p. 3003 - 3007 (2019/05/10)

A highly regioselective Pd-catalyzed carboxyl directed decarboxylative ortho-C-H halogenation of cheap o-nitrobenzoic acids with NaX (X = I, Br) under aerobic conditions has been established. The utility of the method has been demonstrated by the gram-scale reaction and derivatization of the product. Experimental results have confirmed Pd and Bi played critical roles in the transformation and indicated the transformation might proceed via 2-halo-6-nitrobenzoic acid derivative intermediate.

AURORA AND FLT3 KINASES MODULATORS

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Paragraph 0177; 0178, (2015/02/18)

The invention provides a compound having the formula (1): and salts thereof; wherein: R1 is hydrogen or C1-2 alkyl; and R2, R3 and R4 are the same or different and each is selected from hydrogen, C1-2 alkyl, fluorine, chlorine, C1-2 alkoxy and trifluoromethyl, provided that no more than two of R2, R3 and R4 are other than hydrogen. Also provided are pharmaceutical compositions containing the compounds and their use in medicine, and in particular in the treatment of cancer.

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