862287-27-2 Usage
General Description
"(1S,2S)-Methyl 2-amino cyclopentanecarboxylate" is a chemical compound with a molecular formula of C7H13NO2. It is a stereochemically pure derivative of amino cyclopentanecarboxylic acid. (1S,2S)-Methyl 2-aMinocyclopentanecarboxylate is used as a building block in the synthesis of various pharmaceuticals, especially those for the treatment of central nervous system disorders. It is also used as a chiral resolving agent and in the synthesis of other chiral compounds. Additionally, it has potential applications in the field of medicinal chemistry and drug discovery. The compound has a unique stereochemical configuration, making it a valuable component in the development of pharmaceuticals and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 862287-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,2,8 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 862287-27:
(8*8)+(7*6)+(6*2)+(5*2)+(4*8)+(3*7)+(2*2)+(1*7)=192
192 % 10 = 2
So 862287-27-2 is a valid CAS Registry Number.
862287-27-2Relevant articles and documents
Self-condensation of N-tert-butanesulfinyl aldimines: Application to the rapid asymmetric synthesis of biologically important amine-containing compounds
Schenkel, Laurie B.,Ellman, Jonathan A.
, p. 3621 - 3624 (2007/10/03)
(Chemical Equation Presented) Highly diastereoselective intra- and intermolecular self-condensation reactions of N-tert-butanesulfinyl aldimines have been developed and applied to the rapid, asymmetric synthesis of frans-2-aminocyclopentanecarboxylic acid and the drug candidate SC-53116. Key to both syntheses is a novel microwave-assisted reaction in which N-sulfinyl aldimines are cleanly converted into nitrites in high-yielding concerted elimination processes.
