39199-37-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chloroethyl)-2-methylbenzene is used as an intermediate for the synthesis of various pharmaceuticals. Its reactivity, stemming from the chloroethyl group, allows for its involvement in the creation of a wide range of medicinal compounds.
Used in Dye Industry:
In the dye industry, 1-(2-chloroethyl)-2-methylbenzene serves as an intermediate in the production of different types of dyes. Its chemical structure makes it a valuable component in the formulation of colorants for various applications.
Used in Organic Synthesis:
1-(2-chloroethyl)-2-methylbenzene is also utilized as a reactive intermediate in organic synthesis, where it can be further transformed into other valuable organic compounds through chemical reactions.
Used as a Solvent:
Due to its liquid state and chemical properties, 1-(2-chloroethyl)-2-methylbenzene is employed as a solvent in certain chemical processes. Its ability to dissolve other substances makes it a useful component in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39199-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39199-37:
(7*3)+(6*9)+(5*1)+(4*9)+(3*9)+(2*3)+(1*7)=156
156 % 10 = 6
So 39199-37-6 is a valid CAS Registry Number.
39199-37-6Relevant academic research and scientific papers
Cascade bio-hydroxylation and dehalogenation for one-pot enantioselective synthesis of optically active β-halohydrins from halohydrocarbons
Cui, Hai-Bo,Xie, Ling-Zhi,Wan, Nan-Wei,He, Qing,Li, Zhi,Chen, Yong-Zheng
supporting information, p. 4324 - 4328 (2019/08/21)
A stereoselective hydroxylation and enantioselective dehalogenation cascade reaction was developed for the synthesis of optically active β-haloalcohols from halohydrocarbons. This cascade system employed P450 and halohydrin dehalogenase as two compatible biocatalysts, allowing a straightforward, greener and efficient access to β-halohydrins with excellent enantioselectivities (98-99%).
Gallium-catalyzed reductive chlorination of carboxylic acids with copper(II) chloride
Sakai, Norio,Nakajima, Takumi,Yoneda, Shinichiro,Konakahara, Takeo,Ogiwara, Yohei
, p. 10619 - 10623 (2015/02/19)
Described herein is the direct chlorination of carboxylic acids using copper(II) chloride via a gallium(III)-catalyzed reduction in the presence of a hydrosiloxane. During this reductive chlorination, the counteranions of CuCl2 functioned as a chloride source.
