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(+)-(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid|15211|134003-04-6

(+)-(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid

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Sku CI15211_5_G
Chem Impex
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Product Information

Product Name
(+)-(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid
Brand Name
Chem Impex
Product Number
15211
CAS
134003-04-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2734525
IUPAC Name
(1R,4S)-4-aminocyclopent-2-ene-1-carboxylic acid
InChI Key
VTCHZFWYUPZZKL-CRCLSJGQSA-N
SMILES
C1C@H(C=CC@H1N)C(=O)O

Description

(+)-(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.

Biochemical Research: It is used in studies related to amino acid metabolism, helping researchers understand the biochemical pathways and potential therapeutic targets.

Organic Synthesis: The compound is employed in organic synthesis reactions, providing a versatile building block for creating complex molecules in the laboratory.

Material Science: It finds applications in the development of novel materials, particularly in creating polymers with enhanced properties for industrial applications.

Food Industry: The compound can be explored for its potential use as a food additive or flavor enhancer, contributing to the development of healthier food products.

References Data Source From Pubchem

Hydrolysis of Lactams
Publication Name: Science of Synthesis
Publication Date: 2015

Probing the steric requirements of the γ-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin
Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2013-02-15
DOI: 10.1016/j.bmc.2012.12.009

4-Aminobutyrate transaminase
Publication Name: Springer Handbook of Enzymes
Publication Date: 2007
DOI: 10.1007/978-3-540-49755-4_53

Enantiomers of cis-constrained and flexible 2-substituted GABA analogues exert opposite effects at recombinant GABA(C) receptors
Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2006-01-15
DOI: 10.1016/j.bmc.2005.08.037

Systemic administration of 1R,4S‐4‐amino‐cyclopent‐2‐ene‐carboxylic acid, a reversible inhibitor of GABA transaminase, blocks expression of conditioned place preference to cocaine and nicotine in rats
Publication Name: Synapse (New York, N.Y.)
Publication Date: 2002-01-31
DOI: 10.1002/syn.10052|10.1002/syn.10052.abs