CAS 4160-80-9
:Dihydro-4-phenyl-2H-pyran-2,6(3H)-dione
Description:
Dihydro-4-phenyl-2H-pyran-2,6(3H)-dione, also known by its CAS number 4160-80-9, is an organic compound characterized by its bicyclic structure that includes a pyran ring fused with a diketone functionality. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and acetone, but may have limited solubility in water. The presence of the phenyl group contributes to its aromatic properties, which can influence its reactivity and interactions with other chemical species. Dihydro-4-phenyl-2H-pyran-2,6(3H)-dione is of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential applications in the development of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the diketone moiety, which can participate in various chemical reactions, including condensation and cyclization processes. Overall, this compound serves as a valuable building block in synthetic organic chemistry.
Formula:C11H10O3
InChI:InChI=1S/C11H10O3/c12-10-6-9(7-11(13)14-10)8-4-2-1-3-5-8/h1-5,9H,6-7H2
InChI key:InChIKey=DNWAYXNMUKHONN-UHFFFAOYSA-N
SMILES:O=C1CC(CC(=O)O1)C2=CC=CC=C2
Synonyms:- 2H-Pyran-2,6(3H)-dione, dihydro-4-phenyl-
- 3-Phenylglutaric anhydride
- Glutaric anhydride, 3-phenyl-
- Dihydro-4-phenyl-2H-pyran-2,6(3H)-dione
- β-Phenylglutaric anhydride
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Found 2 products.
4-Phenyloxane-2,6-dione
CAS:<p>4-Phenyloxane-2,6-dione is a molecule that has two asymmetric carbons. The molecule has been shown to undergo desymmetrization by the Friedel-Crafts acylation and protonation reactions. 4-Phenyloxane-2,6-dione has been used as a chiral catalyst to synthesize an α,β-unsaturated ketone with an unsymmetrical double bond. <br>4-Phenyloxane-2,6-dione can be used for asymmetric synthesis of aldehydes due to its bifunctional nature. This compound is also used in the catalysis of cyclic reactions.</p>Formula:C11H10O3Purity:Min. 95%Molecular weight:190.19 g/mol

