1212065-90-1 Usage
Description
(1R)-1-(2,6-dichloro-3-fluorophenyl)ethan-1-amine is a chiral amine with the molecular formula C8H9Cl2FN. It features a phenyl ring substituted with two chlorine atoms and one fluorine atom, as well as an ethyl group and a primary amine functional group. (1R)-1-(2,6-dichloro-3-fluorophenyl)ethan-1-amine is specifically the right-handed stereoisomer of its enantiomers.
Uses
Used in Pharmaceutical Synthesis:
(1R)-1-(2,6-dichloro-3-fluorophenyl)ethan-1-amine is utilized as an intermediate in the synthesis of pharmaceutical products. Its unique structure and functional groups make it a valuable component in creating various medicinal compounds.
Used in Agrochemical Production:
(1R)-1-(2,6-dichloro-3-fluorophenyl)ethan-1-amine also serves as an intermediate in the production of agrochemicals, contributing to the development of substances that can protect crops and enhance agricultural productivity.
Used in Research and Development:
(1R)-1-(2,6-dichloro-3-fluorophenyl)ethan-1-amine is employed in research and development settings for the study of biological processes. Its involvement in the creation of new molecules with potential medicinal properties highlights its importance in scientific exploration and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 1212065-90-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,0,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1212065-90:
(9*1)+(8*2)+(7*1)+(6*2)+(5*0)+(4*6)+(3*5)+(2*9)+(1*0)=101
101 % 10 = 1
So 1212065-90-1 is a valid CAS Registry Number.
1212065-90-1Relevant articles and documents
Discovery of novel 2-aminopyridine-3-carboxamides as c-Met kinase inhibitors
Zhang, Dengyou,Ai, Jing,Liang, Zhongjie,Li, Chunpu,Peng, Xia,Ji, Yinchun,Jiang, Hualiang,Geng, Meiyu,Luo, Cheng,Liu, Hong
, p. 5169 - 5180 (2012/11/07)
A series of 2-aminopyridine-3-carboxamide derivatives against c-Met were designed and synthesized by employing bioisosteric replacement of heterocyclic moieties with the amide bond. The structure-activity relationship (SAR) at various positions of the sca
