155935-60-7 Usage
Structure
Pyrrolidine ring with two hydroxyl groups and an amino group attached to the third carbon
Chiral center
One
Stereoisomers
Exists as a pair of enantiomers with (2R,3R,4R) configuration being one of the possible stereoisomers
Applications
Potential use in pharmaceutical and chemical industries for asymmetric synthesis, as a chiral resolving agent, and as a building block for the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 155935-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,3 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155935-60:
(8*1)+(7*5)+(6*5)+(5*9)+(4*3)+(3*5)+(2*6)+(1*0)=157
157 % 10 = 7
So 155935-60-7 is a valid CAS Registry Number.
155935-60-7Relevant articles and documents
IOOC route to substituted chiral pyrrolidines. Potential glycosidase inhibitors
Falb, Eliezer,Bechor, Yosi,Nudelman, Abraham,Hassner, Alfred,Albeck, Amnon,Gottlieb, Hugo E.
, p. 498 - 506 (2007/10/03)
Branched-chain five-membered ring aza-sugar analogues, synthesized from amino acids by an intramolecular oxime-olefin cycloaddition reaction, the IOOC route, were found to be selective glycosidase inhibitors. The derivative 2,4(S)-di(hydroxymethyl)-3(S)-aminopyrrolidine, obtained from D-serine, was about 1 order of potency more active than its enantiomer obtained from L- serine.
