CAS 6836-98-2
:Dihydro-3-phenyl-2(3H)-furanone
Description:
Dihydro-3-phenyl-2(3H)-furanone, also known by its CAS number 6836-98-2, is an organic compound characterized by its furanone structure, which features a five-membered lactone ring. This compound typically exhibits a pale yellow to colorless appearance and is known for its pleasant, sweet, and fruity aroma, making it of interest in the flavor and fragrance industries. Its molecular structure includes a phenyl group, contributing to its aromatic properties. Dihydro-3-phenyl-2(3H)-furanone is soluble in organic solvents, such as ethanol and ether, but has limited solubility in water. The compound is often studied for its potential applications in synthetic organic chemistry and as a building block in the synthesis of more complex molecules. Additionally, it may exhibit biological activity, although specific pharmacological properties would require further investigation. Safety data should be consulted to ensure proper handling, as with any chemical substance.
Formula:C10H10O2
InChI:InChI=1/C10H10O2/c11-10-9(6-7-12-10)8-4-2-1-3-5-8/h1-5,9H,6-7H2
InChI key:InChIKey=QGHNDAKWOGAJHS-UHFFFAOYSA-N
SMILES:O=C1C(CCO1)C2=CC=CC=C2
Synonyms:- (±)-Dihydro-3-phenyl-2(3H)-furanone
- 2(3H)-furanone, dihydro-3-phenyl-
- 2-Phenylbutyrolactone
- 3-Phenyldihydro-2(3H)-furanon
- 3-Phenyldihydro-2(3H)-furanone
- 3-Phenyldihydrofuran-2-one
- 3-Phenyloxolan-2-one
- 3-Phenyltetrahydro-2-furanone
- Butyric acid, 4-hydroxy-2-phenyl-, γ-lactone
- α-Phenyl-γ-butyrolactone
- 3-Phenyloxolane-2-one
- 2-FURANONE,4,5-DIHYDRO-3-PHENYL-
- 4,5-Dihydro-3-phenyl-2(3H)-furanone
- 3-Phenyltetrahydrofuran-2-one
- ALPHA-PHENYL-GAMMA-BUTYROLACTONE
- See more synonyms
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Found 3 products.
3-Phenyloxolan-2-one
CAS:Controlled ProductFormula:C10H10O2Color and Shape:NeatMolecular weight:162.1853-Phenyloxolan-2-one
CAS:<p>Phenyloxolan-2-one is a metabolite of glutethimide. It has been shown to produce dose-dependent sedation and hypnosis in rats. It is also a potent inhibitor of the enzyme gamma-aminobutyric acid transaminase, which is responsible for the conversion of GABA to succinic semialdehyde, and may inhibit the formation of gamma-aminobutyric acid from glutamate. Phenyloxolan-2-one can be detected in urine as a metabolite of glutethimide and has been used as an analytical tool for monitoring glutethimide use.</p>Formula:C10H10O2Purity:Min. 95%Molecular weight:162.18 g/mol


