142452-42-4 Usage
Uses
Used in Pharmaceutical Industry:
(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL is used as a chiral building block for the synthesis of pharmaceuticals, leveraging its unique structure to create new drugs with potential therapeutic benefits.
Used in Chemical Industry:
In the chemical industry, (1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL serves as a key intermediate in the production of various organic compounds, taking advantage of its reactive functional groups and chiral properties.
Used in Medicinal Chemistry:
(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL is utilized in medicinal chemistry for exploring its specific biological activities, which may lead to the discovery of new therapeutic agents or mechanisms of action.
Used in Drug Development Research:
(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL is employed in drug development research to study its potential as a precursor for new drug candidates, providing valuable information that can guide the design and synthesis of novel pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 142452-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,5 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142452-42:
(8*1)+(7*4)+(6*2)+(5*4)+(4*5)+(3*2)+(2*4)+(1*2)=104
104 % 10 = 4
So 142452-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H25NO/c22-20(17-12-6-2-7-13-17)19(16-10-4-1-5-11-16)21-18-14-8-3-9-15-18/h1-2,4-7,10-13,18-22H,3,8-9,14-15H2/t19-,20+/m1/s1
142452-42-4Relevant articles and documents
Asymmetric synthesis XVII. New chiral catalysts for the stereocontrolled addition of benzaldehyde by diethylzinc
Li,Jiang,Mi
, p. 1467 - 1474 (2007/10/02)
Enantioselective addition of benzaldehyde with diethylzinc catalyzed by a few classes of new chiral ligands (3a-3h) and their structural relations are disclosed herein. The stereocontrolled syntheses of both (S)- and (R)-1-phenyl-1-propanol are achieved i
Facile Preparation of Some Highly Hindered Chiral 1,2-Diphenyl-2-(N-monoalkyl)amino Alcohols and N-Benzylbornamine
Jian, Li Sheng,Aiqiao, Mi,Guishu, Yang,Yaozhong, Jiang
, p. 1497 - 1503 (2007/10/02)
The preparation of some novel chiral 1,2-diphenyl-2-(N-monoalkyl)amino alcohols by a facile one-pot procedure and the synthesis of N-benzylbornamine by a reduction process are described herein.
