142508-07-4 Usage
Description
(1S,2R)-2-(ISOPROPYLAMINO)-1,2-DIPHENYLETHANOL is a chiral secondary amine with a hydroxyl group and two phenyl rings. It is often used in organic synthesis and medicinal chemistry as a chiral building block for the creation of pharmaceuticals and other biologically active molecules. The isopropylamino group is a common substituent in many drugs and bioactive compounds, and the chiral nature of the molecule makes it especially useful in the creation of enantiomerically pure pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
(1S,2R)-2-(ISOPROPYLAMINO)-1,2-DIPHENYLETHANOL is used as a chiral building block for the creation of pharmaceuticals and other biologically active molecules. Its chiral nature makes it especially useful in the creation of enantiomerically pure pharmaceuticals.
Used in Medicinal Chemistry:
(1S,2R)-2-(ISOPROPYLAMINO)-1,2-DIPHENYLETHANOL is used as a chiral building block in the development of new drugs and bioactive compounds. The isopropylamino group is a common substituent in many drugs and bioactive compounds, making it a valuable component in medicinal chemistry.
Used in Organic Synthesis:
(1S,2R)-2-(ISOPROPYLAMINO)-1,2-DIPHENYLETHANOL is used as a chiral building block in organic synthesis, allowing for the creation of a wide range of enantiomerically pure compounds.
Used in Pharmacological Research:
(1S,2R)-2-(ISOPROPYLAMINO)-1,2-DIPHENYLETHANOL is studied for its potential pharmacological properties, such as analgesic and anticancer effects, making it a promising candidate for further research and development in the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 142508-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,0 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142508-07:
(8*1)+(7*4)+(6*2)+(5*5)+(4*0)+(3*8)+(2*0)+(1*7)=104
104 % 10 = 4
So 142508-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO/c1-13(2)18-16(14-9-5-3-6-10-14)17(19)15-11-7-4-8-12-15/h3-13,16-19H,1-2H3/t16-,17+/m1/s1
142508-07-4Relevant articles and documents
One-pot synthesis of trisubstituted 1,2-amino alcohols from deprotonated α-amino nitriles
Kison, Coralie,Opatz, Till
experimental part, p. 2740 - 2745 (2009/04/07)
A short synthesis of N,1,2-trisubstituted vicinal amino alcohols by 1,2-addition of deprotonated N-monosubstituted α-amino nitriles to aldehydes and subsequent one-pot reduction of the intermediates with borane-THF is described. This procedure leads to the predominant formation of the anti-configured products. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
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.