159694-26-5 Usage
Description
Pyrrolidine-3,4-dicarboxylic acid is a naturally occurring chemical compound characterized by a pyrrolidine ring with two carboxylic acid groups at the 3 and 4 positions. It is found in certain proteins and functions as a neurotransmitter in the brain, playing a crucial role in the regulation of glutamate receptors. Pyrrolidine-3,4-dicarboxylic acid is implicated in synaptic plasticity, learning, and memory processes, and has been the subject of research for its potential therapeutic applications in various neurological conditions.
Uses
Used in Pharmaceutical Industry:
Pyrrolidine-3,4-dicarboxylic acid is used as a target for drug development for its potential therapeutic applications in treating neurological conditions such as epilepsy, schizophrenia, and neurodegenerative diseases. Its role in the regulation of glutamate receptors and its involvement in synaptic plasticity, learning, and memory make it a promising candidate for the development of new treatments.
Used in Neuroscientific Research:
In the field of neuroscientific research, Pyrrolidine-3,4-dicarboxylic acid is utilized as a tool to study the mechanisms of synaptic plasticity, learning, and memory, as well as to investigate the pathophysiology of neurological disorders. Understanding its role in these processes can provide insights into the development of novel therapeutic strategies for various brain-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 159694-26-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,6,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159694-26:
(8*1)+(7*5)+(6*9)+(5*6)+(4*9)+(3*4)+(2*2)+(1*6)=185
185 % 10 = 5
So 159694-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO4/c8-5(9)3-1-7-2-4(3)6(10)11/h3-4,7H,1-2H2,(H,8,9)(H,10,11)
159694-26-5Relevant articles and documents
A mild Boc deprotection and the importance of a free carboxylate
Thaqi, Ali,McCluskey, Adam,Scott, Janet L.
supporting information; experimental part, p. 6962 - 6964 (2009/04/07)
We report a facile and rapid removal of Boc protecting groups using microwave heating in H2O, with deprotection only requiring a free carboxylic acid group in the starting material. Unlike previous approaches, no additional reagents are required.
