117836-26-7 Usage
Description
(2S,5S)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester is a piperidine derivative, a heterocyclic organic compound with diverse biological activities. It is a methyl benzyl ester of a piperidine dicarboxylic acid, featuring a hydroxy group at the 5th position. (2S,5S)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester is known for its potential as a neurotransmitter modulator and therapeutic agent, warranting further research into its pharmacological and physiological effects.
Uses
Used in Pharmaceutical Industry:
(2S,5S)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester is used as a potential therapeutic agent for its diverse biological activities. Its role as a neurotransmitter modulator makes it a candidate for the development of treatments targeting neurological disorders and other conditions that may benefit from modulation of neurotransmission.
Used in Research Applications:
In the field of scientific research, (2S,5S)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester serves as a valuable compound for studying the structure-activity relationships of piperidine derivatives. This aids in understanding their interactions with biological targets and contributes to the advancement of drug discovery and development processes.
Check Digit Verification of cas no
The CAS Registry Mumber 117836-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117836-26:
(8*1)+(7*1)+(6*7)+(5*8)+(4*3)+(3*6)+(2*2)+(1*6)=137
137 % 10 = 7
So 117836-26-7 is a valid CAS Registry Number.
117836-26-7Relevant articles and documents
MANUFACTURING METHOD OF (2S,5S)-5-HYDROXY-2-PIPERIDINECARBOXYLIC ACID AS WELL AS MANUFACTURING INTERMEDIATE OF THE SAME AND METHOD FOR MANUFACTURING THE SAME
-
, (2016/12/22)
PROBLEM TO BE SOLVED: To provide synthesis methods of 5-hydroxy-6-methoxypiperidine-2-carboxylic acid derivatives and 5-oxopiperidine-2-carboxylic acid derivatives more safely than ever by using inexpensive raw ingredients. SOLUTION: In the provided method, a compound expressed by the following formula [X] is manufactured from a compound expressed by the following formula [I] through steps (1) through (9) [either steps (4) and (5) or steps (6) and (7) in the case of steps (4) through (7)]. COPYRIGHT: (C)2015,JPOandINPIT
CHIRAL SYNTHESIS OF 5-HYDROXY-(L)-PIPECOLIC ACIDS FROM (L)-GLUTAMIC ACID
Bailey, Patrick D.,Bryans, Justin S.
, p. 2231 - 2234 (2007/10/02)
A stereo- and enantio-specific synthesis of the naturally occuring cis-5-hydroxy-(L)-pipecolic acid (3) is described, starting from Z-(L)-glutamic acid; the key step involves cyclisation of a protected chlorohydrin, and also gives access to trans-5-hydroxy-(L)-pipecolic acid.