151412-12-3 Usage
Description
2-Fluoro-3-methylbenzyl bromide is an organic compound that serves as a chemical and organic intermediate. It is characterized by its clear colorless to light yellow liquid appearance after synthesis.
Uses
Used in Chemical Industry:
2-Fluoro-3-methylbenzyl bromide is used as a chemical intermediate for the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows it to be a versatile building block in the development of new molecules with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-fluoro-3-methylbenzyl bromide is used as a key intermediate in the production of drugs with specific therapeutic properties. Its fluorinated and methylated structure can contribute to the enhancement of the drug's efficacy, selectivity, and pharmacokinetic profile.
Used in Research and Development:
2-Fluoro-3-methylbenzyl bromide is also utilized in research and development settings for the exploration of new chemical reactions and the synthesis of novel compounds with potential applications in various industries, including materials science, agrochemicals, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 151412-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,1 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151412-12:
(8*1)+(7*5)+(6*1)+(5*4)+(4*1)+(3*2)+(2*1)+(1*2)=83
83 % 10 = 3
So 151412-12-3 is a valid CAS Registry Number.
151412-12-3Relevant articles and documents
Synthesis of Phenanthridines through Palladium-Catalyzed Cascade Reaction of 2-Halo-N-Ms-arylamines with Benzyl Halides/Sulfonates
Yang, Si-Yi,Han, Wen-Yong,Zhang, Ding-Lei,Zhou, Xiao-Jian,Bai, Mei,Cui, Bao-Dong,Wan, Nan-Wei,Yuan, Wei-Cheng,Chen, Yong-Zheng
, p. 996 - 1003 (2017/02/15)
An efficient palladium-catalyzed nucleophilic substitution/C–H activation/aromatization cascade reaction between readily available 2-halo-N-Ms-arylamines (Ms = methanesulfonyl) and benzyl halides/sulfonates has been described. A wide variety of phenanthridines were synthesized in a one-pot fashion in moderate to high yields (37–86 %). Notably, this method provides a straightforward, facile approach for the synthesis of phenanthridines. The practicality was further substantiated by successfully carrying out a gram-scale preparation.
