862287-27-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(1S,2S)-Methyl 2-amino cyclopentanecarboxylate is utilized as a building block in the synthesis of various pharmaceuticals, particularly those targeting the treatment of central nervous system disorders. Its unique stereochemistry plays a crucial role in the development of these medications.
Used as a Chiral Resolving Agent:
In the field of chemistry, (1S,2S)-Methyl 2-amino cyclopentanecarboxylate serves as a chiral resolving agent. This function is essential for separating enantiomers, which are molecules that are mirror images of each other but may have different biological activities.
Used in the Synthesis of Chiral Compounds:
(1S,2S)-Methyl 2-aMinocyclopentanecarboxylate is also employed in the synthesis of other chiral compounds, which are vital for various applications in the chemical and pharmaceutical industries. Chiral compounds are important due to their specific interactions with biological systems, often exhibiting different effects based on their stereochemistry.
Used in Medicinal Chemistry and Drug Discovery:
(1S,2S)-Methyl 2-amino cyclopentanecarboxylate holds potential applications in the field of medicinal chemistry and drug discovery. Its unique properties and stereochemistry make it a promising candidate for the development of new drugs and therapeutic agents.
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.
Synthesis of Cyclic β-Amino Acid Esters from Methionine, Allylglycine, and Serine
Gardiner, James,Anderson, Kelly H.,Downard, Alison,Abell, Andrew D.
, p. 3375 - 3382 (2007/10/03)
Here we report a versatile ring-closing metathesis-based approach to 5-, 6-, and 7-membered cyclic β-amino esters starting with simple and readily available building blocks-methionine, allylglycine, and serine-where the nature of the amino acid determines
