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2-Bromo-5-chloro-p-xylene, with the molecular formula C8H7BrCl, is a substituted aromatic hydrocarbon that incorporates both bromine and chlorine atoms. It is a versatile chemical compound known for its significant role in the field of organic chemistry and chemical synthesis.

85072-44-2

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85072-44-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-5-chloro-p-xylene is used as a building block in the synthesis of biologically active compounds for the pharmaceutical industry. Its unique structure allows for the creation of various medicinal agents, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-5-chloro-p-xylene serves as a precursor for the production of agrochemicals, playing a vital role in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Synthesis:
2-Bromo-5-chloro-p-xylene is utilized as an intermediate in the manufacturing of organic chemicals, facilitating the synthesis of a wide range of organic compounds for various applications.
Used in Dye and Pigment Production:
This chemical compound is also used as a precursor for the production of dyes and pigments, contributing to the coloration and appearance of various products in different industries.
Used in Research and Industrial Processes:
2-Bromo-5-chloro-p-xylene functions as a reagent in numerous research and industrial processes, enabling the exploration of new chemical reactions and the advancement of chemical technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 85072-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,7 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85072-44:
(7*8)+(6*5)+(5*0)+(4*7)+(3*2)+(2*4)+(1*4)=132
132 % 10 = 2
So 85072-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrCl/c1-5-4-8(10)6(2)3-7(5)9/h3-4H,1-2H3

85072-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-chloro-2,5-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 2-bromo-5-chloro-p-xylene

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:85072-44-2 SDS

85072-44-2Relevant academic research and scientific papers

N-SULFONYL BENZAMIDE DERIVATIVE WITH HETEROCYCLIC SUBSTITUENT, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF

-

Paragraph 0158; 0159, (2019/01/04)

The present invention discloses an N-sulfonyl benzamide derivative with a heterocyclic substituent, and a preparation method therefor and a pharmaceutical application thereof. More specifically, the invention discloses a compound represented by formula (II) or a pharmaceutically acceptable salt, stereoisomer, solvent compound, or prodrug thereof, and a preparation method therefor and an application thereof. Refer to the specification for definitions of each group in the formula.

Synthesis and Characterization of Two Unsymmetrical Indenofluorene Analogues: Benzo[5,6]-s-indaceno[1,2-b]thiophene and Benzo[5,6]-s-indaceno[2,1-b]thiophene

Marshall, Jonathan L.,Oneal, Nathaniel J.,Zakharov, Lev N.,Haley, Michael M.

, p. 3674 - 3680 (2016/05/24)

The synthesis and characterization of two benzo-indaceno-thiophene compounds (anti-BIT and syn-BIT) are described. Two sequential Suzuki cross-couplings utilizing the halogen selectivity of this reaction permit modular assembly of unsymmetrical indeno[1,2

Iterative Reductive Aromatization/Ring-Closing Metathesis Strategy toward the Synthesis of Strained Aromatic Belts

Golder, Matthew R.,Colwell, Curtis E.,Wong, Bryan M.,Zakharov, Lev N.,Zhen, Jingxin,Jasti, Ramesh

supporting information, p. 6577 - 6582 (2016/06/09)

The construction of all sp2-hybridized molecular belts has been an ongoing challenge in the chemistry community for decades. Despite numerous attempts, these double-stranded macrocycles remain outstanding synthetic challenges. Prior approaches

Process for the nuclear chlorination of toluene

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, (2008/06/13)

Para-chlorotoluene is prepared selectively at high yield by nuclear chlorination of toluene, in the presence of a Lewis acid catalyst, and a co-catalyst comprising at least one compound selected from the group consisting of phenoxthine derivatives and hig

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