(1S,4R)-4-Amino-2-cyclopentene-1-carboxylic Acid Methyl Ester (2R,3R)-2,3-Dihydroxybutanedioate

Product Name (1S,4R)-4-Amino-2-cyclopentene-1-carboxylic Acid Methyl Ester (2R,3R)-2,3-Dihydroxybutanedioate
CAT No. CS-T-47721
CAS No. 419563-22-7
Category Impurities
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles COC(=O)C1CC(C=C1)N.C(C(C(=O)O)O)(C(=O)O)O
InchIKey XSEHIOOHMZAFCV-IBSOYGIKSA-N
Inchl InChI=1S/C7H11NO2.C4H6O6/c1-10-7(9)5-2-3-6(8)4-5;5-1(3(7)8)2(6)4(9)10/h2-3,5-6H,4,8H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t5-,6+;1-,2-/m11/s1
IUPAC (2R,3R)-2,3-dihydroxybutanedioic acid;methyl (1S,4R)-4-aminocyclopent-2-ene-1-carboxylate
Controlled No
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(1S,4R)-4-Amino-2-cyclopentene-1-carboxylic Acid Methyl Ester (2R,3R)-2,3-Dihydroxybutanedioate is a complex organic compound used in various chemical and biological applications. It is commonly known as ACPC and is a chiral compound with two stereocenters. The compound is a derivative of proline and is used in the synthesis of peptides and protein analogs. ACPC has a unique chemical structure that allows it to play a vital role in several biological processes. It acts as an agonist for the glycine receptor and can modulate the activity of the NMDA receptor. As such, it is extensively used in pharmacological research to study the mechanisms of these receptors. Additionally, the compound has been found to exhibit anticonvulsant and neuroprotective properties, making it a promising candidate for the treatment of neurological disorders. ACPC is also used

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