CAS 41371-53-3
:2-imidazolidone-4-carboxylic acid
Description:
2-Imidazolidone-4-carboxylic acid, also known by its CAS number 41371-53-3, is an organic compound characterized by its imidazolidone structure, which features a five-membered ring containing two nitrogen atoms. This compound is a derivative of imidazolidone, with a carboxylic acid functional group at the 4-position, contributing to its acidic properties. It is typically a white to off-white crystalline solid that is soluble in water and polar organic solvents, making it useful in various chemical applications. The presence of both the imidazolidone ring and the carboxylic acid group allows for potential interactions in biological systems, which may lead to applications in pharmaceuticals or biochemistry. Additionally, its unique structure may impart specific reactivity, making it a candidate for further chemical modifications or as a building block in synthetic organic chemistry. As with many chemical substances, handling should be done with care, following appropriate safety guidelines to mitigate any potential hazards.
Formula:C4H6N2O3
InChI:InChI=1/C4H6N2O3/c7-3(8)2-1-5-4(9)6-2/h2H,1H2,(H,7,8)(H2,5,6,9)/t2-/m0/s1
SMILES:C1[C@@H](C(=O)O)NC(=N1)O
Synonyms:- 2-Imidazolidine-4-carboxylic acid
- L-2-Imidazolidone-4-carboxylic acid
- 4-Imidazolidinecarboxylic acid, 2-oxo-, (S)-
- (4S)-2-oxoimidazolidine-4-carboxylic acid
- 2-Imidazolidone-4-carboxylic acid
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Found 5 products.
2-IMIDAZOLIDONE-4-CARBOXYLIC ACID
CAS:Formula:C4H6N2O3Purity:97%Color and Shape:SolidMolecular weight:130.1020(S)-2-Oxoimidazolidine-4-carboxylic acid
CAS:<p>(S)-2-Oxoimidazolidine-4-carboxylic acid</p>Purity:97%Molecular weight:130.10204g/mol(4S)-2-oxoimidazolidine-4-carboxylic Acid
CAS:Controlled ProductFormula:C4H6N2O3Color and Shape:NeatMolecular weight:130.1022-Oxoimidazolidine-4-carboxylic acid
CAS:<p>2-Oxoimidazolidine-4-carboxylic acid is an inhibitor of matrix metalloproteinases. It inhibits the activity of these enzymes by binding to the zinc ion, which is necessary for the enzyme's activity. 2-Oxoimidazolidine-4-carboxylic acid has been shown to inhibit ulceration in rats, and it has also been shown to decrease expression of glutamate receptors in mice. This drug also inhibits amino acid transport by competing with amino acids for transport across the blood brain barrier and binds to serine protease, which prevents proteolytic degradation of proteins in the extracellular matrix. 2-Oxoimidazolidine-4-carboxylic acid also inhibits acid transport and cancer cell proliferation.</p>Formula:C4H6N2O3Purity:Min. 95%Molecular weight:130.1 g/mol




