137442-19-4 Usage
Description
(R)-4-benzylpiperazine-2-carboxylic acid is a chiral chemical compound belonging to the class of piperazine derivatives. It possesses a unique structure that has been studied for its potential pharmacological properties, particularly as a ligand for certain receptors in the central nervous system. This structure also makes it a promising candidate for further research in medicinal chemistry and pharmacology.
Uses
Used in Pharmaceutical Industry:
(R)-4-benzylpiperazine-2-carboxylic acid is used as a potential ligand for [application reason] its pharmacological properties and interactions with receptors in the central nervous system. This makes it a valuable compound for drug design and development, particularly in the context of central nervous system disorders.
Used in Medicinal Chemistry Research:
(R)-4-benzylpiperazine-2-carboxylic acid is used as a research compound for [application reason] its unique structure and potential pharmacological properties. This allows scientists to explore its interactions with various receptors and its potential applications in the development of new medications.
Used in Drug Design and Development:
(R)-4-benzylpiperazine-2-carboxylic acid is used as a starting point for [application reason] its potential as a ligand and its structural properties. This enables researchers to modify and optimize its structure to create new drugs with improved efficacy and selectivity for specific targets in the central nervous system.
Check Digit Verification of cas no
The CAS Registry Mumber 137442-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137442-19:
(8*1)+(7*3)+(6*7)+(5*4)+(4*4)+(3*2)+(2*1)+(1*9)=124
124 % 10 = 4
So 137442-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O2/c15-12(16)11-9-14(7-6-13-11)8-10-4-2-1-3-5-10/h1-5,11,13H,6-9H2,(H,15,16)/t11-/m1/s1
137442-19-4Relevant articles and documents
Enantiomerically pure 2-piperazinemethanols as novel chiral ligands of oxazaborolidine catalysts in enantioselective borane reductions
Inoue, Tsutomu,Sato, Daisuke,Komura, Kenichi,Itsuno, Shinichi
, p. 5379 - 5382 (1999)
Novel enantiomerically pure 2-piperazinemethanols (3-5) were synthesized from 2-piperazinecarboxylic acid 1. The asymmetric reduction of aromatic ketones, ketimine and oxime ether has been performed with reagents prepared from 2-piprazinemethanol and borane to yield enantiomerically enriched alcohols and amines, respectively. The preferred absolute configuration of the product was dependent on the structure of the sulfonyl substituent in the chiral ligand.