142452-42-4 Usage
General Description
"(1S,2R)-2-(cyclohexylamino)-1,2-diphenylethanol" is a chemical compound with a unique structure consisting of a cyclohexylamino group attached to a chiral carbon center, along with two phenyl groups. (1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL has potential applications in the pharmaceutical and chemical industries due to its chiral nature and potential for use as a building block in the synthesis of various pharmaceuticals and other organic compounds. It may also have specific biological activities that could make it useful in medicinal chemistry. The synthesis and study of (1S,2R)-2-(cyclohexylamino)-1,2-diphenylethanol could provide valuable information for the development of new drugs and materials.
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
