CAS 14825-82-2
:(S)-(-)-4-Benzyloxazolidine-2,5-dione
Description:
(S)-(-)-4-Benzyloxazolidine-2,5-dione, also known as (S)-(-)-benzyl oxazolidine-2,5-dione, is a chiral compound characterized by its oxazolidine ring structure, which contains both a carbonyl and an ether functional group. This compound is typically a white to off-white solid and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water. Its chirality is significant in pharmaceutical applications, as it can exhibit different biological activities depending on its stereochemistry. The compound is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the development of chiral building blocks. Additionally, it may participate in reactions such as nucleophilic substitutions and cycloadditions, making it valuable in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C10H9NO3
InChI:InChI=1/C10H9NO3/c12-9-8(11-10(13)14-9)6-7-4-2-1-3-5-7/h1-5,8H,6H2,(H,11,13)/t8-/m0/s1
SMILES:c1ccc(cc1)C[C@H]1C(=O)OC(=N1)O
Synonyms:- L-Phenylalanine N-carboxyanhydride
- (4S)-4-benzyl-1,3-oxazolidine-2,5-dione
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Found 4 products.
2,5-Oxazolidinedione, 4-(phenylmethyl)-, (4S)-
CAS:Formula:C10H9NO3Purity:95%Color and Shape:SolidMolecular weight:191.1834L-phenylalanine N-carboxyanhydride
CAS:Formula:C10H9NO3Purity:95%Color and Shape:SolidMolecular weight:191.186(4S)-4-benzyl-1,3-oxazolidine-2,5-dione
CAS:<p>This compound is a model for the study of hydroxyapatite. The (4S)-4-benzyl-1,3-oxazolidine-2,5-dione has been shown to be an effective macroinitiator for ring-opening polymerization. It can be used as a biological marker for bone growth factor. The compound has also been shown to have antiinflammatory properties in both animal and cell culture studies.</p>Formula:C10H9NO3Purity:Min. 95%Molecular weight:191.18 g/mol
