CAS 7480-32-2
:4-phenyl-1,3-oxazolidin-2-one
Description:
4-Phenyl-1,3-oxazolidin-2-one, with the CAS number 7480-32-2, is a heterocyclic organic compound characterized by its oxazolidinone structure, which features a five-membered ring containing both nitrogen and oxygen atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. It is known for its potential applications in medicinal chemistry, particularly as a scaffold in the development of pharmaceuticals due to its ability to mimic amino acids and peptides. The presence of the phenyl group contributes to its aromatic properties, which can influence its reactivity and interactions with biological targets. Additionally, 4-phenyl-1,3-oxazolidin-2-one may exhibit interesting biological activities, including antimicrobial and anti-inflammatory effects, making it a subject of interest in drug discovery. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.
Formula:C9H9NO2
InChI:InChI=1/C9H9NO2/c11-9-10-8(6-12-9)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,10,11)
SMILES:c1ccc(cc1)C1COC(=N1)O
Synonyms:- 2-Oxazolidinone, 4-Phenyl-
- 4-Phenyl-1,3-oxazolidin-2-one
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Found 5 products.
4-Phenyl-1,3-oxazolidin-2-one
CAS:<p>4-Phenyl-1,3-oxazolidin-2-one</p>Purity:98%Molecular weight:163.17g/mol4-Phenyloxazolidin-2-one
CAS:<p>4-Phenyloxazolidin-2-one is a biologically active compound that is activated by hydrochloride salts to form 4-phenyloxazolidin-2,4-dione. This compound can be used as a monosubstituted, enantiopure, or racemic mixture of the two stereoisomers. It is also available in an enantiopure form that has been synthesized through a triphosgene reaction. The vibrational, nmr spectra and functional groups are also studied to determine the chemical structure of this molecule.</p>Formula:C9H9NO2Purity:Min. 95%Molecular weight:163.18 g/mol
