171866-64-1 Usage
Description
(S)-Homopipecolicacidmethylester, also known as (S)-methyl homopipecolate, is a chiral chemical compound characterized by its piperidine ring, carboxylic acid group, and a methyl ester group. This molecule is known for its specific three-dimensional arrangement of atoms, which makes it a valuable asset in organic synthesis and pharmaceutical research. Its ability to interact with biological targets and modulate biological processes renders it a promising candidate for the development of drugs and other bioactive molecules.
Uses
Used in Pharmaceutical Research:
(S)-Homopipecolicacidmethylester is used as a building block for the synthesis of various bioactive compounds, playing a crucial role in the development of new drugs and therapeutic agents. Its interaction with biological targets and potential to modulate biological processes make it a valuable tool in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-Homopipecolicacidmethylester serves as an important intermediate for the creation of a wide range of chemical compounds. Its unique structure and functional groups facilitate the synthesis of complex molecules, contributing to the advancement of chemical research and development.
Used in Drug Development:
(S)-Homopipecolicacidmethylester is used as a key component in the development of new drugs, particularly those targeting specific biological processes. Its chiral nature and ability to interact with biological targets make it a versatile and promising molecule for the creation of innovative pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 171866-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 171866-64:
(8*1)+(7*7)+(6*1)+(5*8)+(4*6)+(3*6)+(2*6)+(1*4)=161
161 % 10 = 1
So 171866-64-1 is a valid CAS Registry Number.
171866-64-1Relevant articles and documents
Chemoenzymatic approach to enantiopure piperidine-based β-amino esters in organic solvents
Liljeblad, Arto,Kavenius, Hanna-Maija,Taehtinen, Petri,Kanerva, Liisa T.
, p. 181 - 191 (2007/10/03)
This research concentrates on the enantioselectivities of lipase-catalysed reactions with methyl esters of 2-piperidylacetic acid and 3-piperidinecarboxylic acid derivatives. N-Acetylated 2-piperidylacetic acid methyl ester displayed good enantioselectivi
Chiral heterocyclic β-enamino esters: Convenient synthesis and diastereoselective reduction
Calvet, Sandrine,David, Olivier,Vanucci-Bacqué, Corinne,Fargeau-Bellassoued, Marie-Claude,Lhommet, Gérard
, p. 6333 - 6339 (2007/10/03)
The preparation of chiral pyrrolidine and piperidine β-enamino esters starting from ω-halogeno β-keto esters, their diastereoselective reduction and the subsequent cleavage of the chiral auxiliary are described.
Ring closing metathesis for the asymmetric synthesis of (S)-homopipecolic acid, (S)-homoproline and (S)-coniine
Davies, Stephen G.,Iwamoto, Keiji,Smethurst, Christian A. P.,Smith, Andrew D.,Rodriguez-Solla, Humberto
, p. 1146 - 1148 (2007/10/03)
Diastereoselective conjugate addition of lithium (S)-N-allyl-N-α-methylbenzylamide to α,β-unsaturated esters or Weinreb amides, followed by ring closing metathesis is used to afford the cyclic β-amino acids (S)-homopipecolic acid and (S)-homoproline and the amine (S)-coniine in high ee.
