400090-60-0 Usage
General Description
(R)-3-aminopentanenitrile is a chemical compound with the molecular formula C5H10N2. It is a chiral compound, meaning it has a non-superimposable mirror image. (R)-3-AMINOPENTANENITRILE is an aminonitrile, which is a class of organic compounds that contain both an amine and a nitrile functional group. (R)-3-aminopentanenitrile is used in various chemical processes and as a building block in the synthesis of pharmaceuticals and other organic compounds. It is also used in the production of agrochemicals and as an intermediate in the synthesis of other complex organic molecules. The compound's chiral nature allows it to be used as a precursor for the synthesis of chiral drugs and other biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 400090-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,0,9 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 400090-60:
(8*4)+(7*0)+(6*0)+(5*0)+(4*9)+(3*0)+(2*6)+(1*0)=80
80 % 10 = 0
So 400090-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2/c1-2-5(7)3-4-6/h5H,2-3,7H2,1H3/t5-/m1/s1
400090-60-0Relevant articles and documents
Asymmetric synthesis of the cholesteryl ester transfer protein inhibitor torcetrapib
Damon, David B.,Dugger, Robert W.,Hubbs, Stephen E.,Scott, Jill M.,Scott, Robert W.
, p. 472 - 480 (2012/12/22)
Previously our group reported synthetic efforts used to synthesize kilogram quantities of the cholesteryl ester transfer protein (CETP) inhibitor torcetrapib, 1, via a mid-stage resolution. This account describes research conducted to develop an asymmetri
BIOCATALYTIC PREPARATION OF ENANTIOMERICALLY ENRICHED AMINOPENTANENITRILE
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Page 10; 11; 12, (2010/02/07)
Methods for preparing enantiomerically enriched aminopentanenitriles are provided. The methods involve selective acylation of an enantiomeric mixture of 3-aminopentanenitrile or selective hydrolysis of an enantiomeric mixture of 3-aminopentanenitrile amide in the presence of an enzyme selected from the group comprising lipase, esterase, and acylase. The methods yield R-aminopentanenitrile, which can be used to produce pharmaceutical products.
