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1-(bromomethyl)-2-chloro-4-methylbenzene, also known as 2-chloro-1-(bromomethyl)-4-methylbenzene, is a chemical compound with the molecular formula C8H8ClBr. It is a derivative of benzene, featuring a chlorine atom, a bromine atom, and a methyl group attached to the benzene ring. 1-(bromomethyl)-2-chloro-4-methylbenzene is utilized in various chemical processes and has potential applications across different industries.

868860-20-2

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868860-20-2 Usage

Uses

Used in Organic Synthesis:
1-(bromomethyl)-2-chloro-4-methylbenzene is used as a starting material for the production of other compounds in the field of organic synthesis. Its unique structure allows for further chemical reactions and modifications, making it a valuable component in creating a wide range of chemical products.
Used in Research:
1-(bromomethyl)-2-chloro-4-methylbenzene serves as a reagent in various chemical reactions, making it an essential tool in research laboratories. It aids scientists in understanding the behavior of different chemical substances and contributes to the development of new chemical processes and products.
Used in Pharmaceutical Industry:
1-(bromomethyl)-2-chloro-4-methylbenzene has potential applications in the pharmaceutical industry, where it can be used to develop new drugs or improve the synthesis of existing ones. Its unique chemical properties make it a promising candidate for creating novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(bromomethyl)-2-chloro-4-methylbenzene can be employed in the development of new pesticides, herbicides, or other agricultural chemicals. Its versatility in chemical reactions allows for the creation of targeted and effective products for the agricultural sector.
Used in Polymer Production:
1-(bromomethyl)-2-chloro-4-methylbenzene is also used in the production of polymers and other industrial chemicals. Its chemical structure can be manipulated to create polymers with specific properties, making it a valuable asset in the development of new materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 868860-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,8,6 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 868860-20:
(8*8)+(7*6)+(6*8)+(5*8)+(4*6)+(3*0)+(2*2)+(1*0)=222
222 % 10 = 2
So 868860-20-2 is a valid CAS Registry Number.

868860-20-2Downstream Products

868860-20-2Relevant academic research and scientific papers

A new protocol for the synthesis of 4,7,12,15-tetrachloro[2.2]paracyclophane

Pan, Donghui,Wang, Yanbin,Xiao, Guomin

, p. 2443 - 2449 (2016/12/07)

We report a green and convenient protocol to prepare 4,7,12,15-tetrachloro[2.2]paracyclophane, the precursor of parylene D, from 2,5-dichloro-p-xylene. In the first bromination step, with H2O2-HBr as a bromide source, this procedure becomes organic-waste-free and organic-solvent-free and can appropriately replace the existing bromination methods. The Winberg elimination-dimerization step, using aqueous sodium hydroxide solution instead of silver oxide for anion exchange, results in a significant improvement in product yield. Furthermore, four substituted [2.2]paracyclophanes were also prepared in this convenient way.

Triazole containing novobiocin and biphenyl amides as Hsp90 C-terminal inhibitors

Zhao, Jinbo,Zhao, Huiping,Hall, Jessica A.,Brown, Douglas,Brandes, Eileen,Bazzill, Joseph,Grogan, Patrick T.,Subramanian, Chitra,Vielhauer, George,Cohen, Mark S.,Blagg, Brian S. J.

supporting information, p. 1317 - 1323 (2014/10/15)

Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due to their ability to segregate client protein degradation from induction of the prosurvival heat shock response, which is a major detriment associated with

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