39199-36-5 Usage
Uses
Used in Chemical Industry:
1-(2-chloroethyl)-3-methylbenzene is used as an intermediate in the synthesis of various chemical compounds for [application reason]. Its unique structure allows for further functionalization and modification, making it a valuable building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
1-(2-chloroethyl)-3-methylbenzene is used as a starting material in the development of new drugs for [application reason]. Its aromatic nature and the presence of a chlorine atom make it a suitable candidate for the synthesis of novel therapeutic agents with potential applications in the treatment of various diseases.
Used in Agrochemical Industry:
1-(2-chloroethyl)-3-methylbenzene is used as a precursor in the production of agrochemicals for [application reason]. Its chemical properties enable the creation of new pesticides, herbicides, or insecticides that can be more effective and environmentally friendly compared to existing products.
Used in Research and Development:
1-(2-chloroethyl)-3-methylbenzene is used as a research compound in academic and industrial laboratories for [application reason]. Its reactivity and structural features make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and discovering new applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 39199-36-5 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 39199-36:
(7*3)+(6*9)+(5*1)+(4*9)+(3*9)+(2*3)+(1*6)=155
155 % 10 = 5
So 39199-36-5 is a valid CAS Registry Number.
39199-36-5Relevant 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%).
