1075715-54-6 Usage
Description
(1S)(3-CHLOROPHENYL)CYCLOPROPYLMETHYLAMINE, with the molecular formula C10H12ClN, is a cyclopropylmethylamine derivative featuring a 3-chlorophenyl group attached to the cyclopropylmethylamine moiety. This chemical compound has been the subject of research for its potential pharmacological activities, particularly as a psychostimulant and a possible treatment for central nervous system disorders. Additionally, it is being explored for its role in the synthesis of pharmaceuticals and other organic compounds. Further research is required to fully understand its properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(1S)(3-CHLOROPHENYL)CYCLOPROPYLMETHYLAMINE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new medications targeting central nervous system disorders.
Used in Research and Development:
In the scientific community, (1S)(3-CHLOROPHENYL)CYCLOPROPYLMETHYLAMINE serves as a subject of study for its potential pharmacological activities, including its psychostimulant effects and its possible role in the treatment of central nervous system disorders, aiding in the advancement of medical knowledge in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 1075715-54-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,7,1 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1075715-54:
(9*1)+(8*0)+(7*7)+(6*5)+(5*7)+(4*1)+(3*5)+(2*5)+(1*4)=156
156 % 10 = 6
So 1075715-54-6 is a valid CAS Registry Number.
1075715-54-6Relevant articles and documents
Kinetic Resolution of Benzylamines via Palladium(II)-Catalyzed C-H Cross-Coupling
Xiao, Kai-Jiong,Chu, Ling,Chen, Gang,Yu, Jin-Quan
, p. 7796 - 7800 (2016)
A Pd(II)-catalyzed enantioselective C-H cross-coupling of benzylamines via kinetic resolution has been achieved using chiral mono-N-protected α-amino-O-methylhydroxamic acid (MPAHA) ligands. Both chiral benzylamines and ortho-arylated benzylamines are obtained in high enantiomeric purity. The use of a readily removable nosyl (Ns) protected amino group as the directing group is a crucial practical advantage. Moreover, the ortho-arylated benzylamine products could be further transformed into chiral 6-substituted 5,6-dihydrophenanthridines as important structural motifs in natural products and bioactive molecules.
