(S)-2-oxoimidazolidine-4-carboxylic acid

(S)-2-oxoimidazolidine-4-carboxylic acid

5-[4-(Difluoromethoxy)phenyl]-5-methylimidazolidine-2,4-dione

5-[4-(Difluoromethoxy)phenyl]-5-methylimidazolidine-2,4-dione

(S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylic acid

$200.00
CAS No.: 59760-01-9
Catalog No.: 192686
Purity: 95%
MF: C12H12N2O5
MW: 264.237
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)OC(=O)N1C(NC[C@H]1C(=O)O)=O
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192686
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(S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylic acid; CAS No.: 59760-01-9; (S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylic acid. PROPERTIES: This Boc-protected oxo acid has molecular formula C12H13NO5. It generally appears as a white crystalline powder. The (S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylic acid exhibits limited water solubility but good solubility in polar aprotic solvents like DMSO and DMF. Its melting point ranges between 160-165 C, and it has a molecular weight of approximately 263.24 g/mol. When handling, care should be taken to avoid skin contact and use of proper respiratory protection. Storage should be in a tightly sealed container at room temperature, protected from light and moisture. The compound is sensitive to strong acids and may undergo Zempl n deprotection upon exposure to aqueous conditions. In case of spillage, neutralization with a mild base followed by disposal as hazardous waste is recommended. APPLICATIONS: The (S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylic acid serves as a key intermediate in the synthesis of peptidomimetic drugs where the carboxylic acid group forms amide bonds with amino acid residues (as detailed in medicinal chemistry literature). The Zempl n protecting group allows for controlled deprotection under mild acidic conditions. Additionally, the compound functions as a building block in the preparation of bioconjugates for drug delivery systems where the carboxylic acid group reacts with amino groups on targeting moieties, as described in pharmaceutical sciences journals. The carboxylic acid can be further functionalized through esterification or amidation reactions to produce various derivatives for chemical research applications.

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