79467-22-4 Usage
Description
2-[2-(AMINOMETHYL)PHENYLTHIO]BENZYL ALCOHOL is an organic compound with a unique chemical structure that features a benzyl alcohol core, an aminomethyl group, and a phenylthio substituent. 2-[2-(AMINOMETHYL)PHENYLTHIO]BENZYL ALCOHOL exhibits a range of properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2-[2-(AMINOMETHYL)PHENYLTHIO]BENZYL ALCOHOL is used as an antidepressant agent for its potential to modulate neurotransmitter levels and alleviate symptoms of depression.
Used in Chemical Synthesis:
2-[2-(AMINOMETHYL)PHENYLTHIO]BENZYL ALCOHOL may be used as an intermediate or building block in the synthesis of other organic compounds, such as pharmaceuticals, agrochemicals, or specialty chemicals, due to its versatile functional groups and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 79467-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,6 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79467-22:
(7*7)+(6*9)+(5*4)+(4*6)+(3*7)+(2*2)+(1*2)=174
174 % 10 = 4
So 79467-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NOS/c15-9-11-5-1-3-7-13(11)17-14-8-4-2-6-12(14)10-16/h1-8,16H,9-10,15H2
79467-22-4Relevant articles and documents
Sequential C-H activation enabled expedient delivery of polyfunctional arenes
Cai, Xiaoqing,Chen, Qian,Chen, Xiaojian,Gao, Yang,Huo, Yanping,Li, Xianwei,Ouyang, Wensen,Rao, Jianhang,Wang, Jie
supporting information, p. 8075 - 8078 (2021/08/20)
Modular construction of polyfunctional arenes from abundant feedstocks stands as an unremitting pursue in synthetic chemistry, accelerating the discovery of drugs and materials. Herein, using the multiple C-H activation strategy with versatile imidate esters, the expedient delivery of molecular libraries of densely functionalized sulfur-containing arenes was achieved, which enabled the concise construction of biologically active molecules, such as Bipenamol.