3-phenyl-5,6-dihydro-2H-pyran-2-one

Base Information

Chemical Name:3-phenyl-5,6-dihydro-2H-pyran-2-one
CAS No.:13019-35-7
Molecular Formula:C₁₁H₁₀O₂
Molecular Weight:174.199
Hs Code.:
DSSTox Substance ID:DTXSID801293440
Nikkaji Number:J1.280.614K

Synonyms:13019-35-7;5,6-dihydro-3-phenyl-2h-pyran-2-one;3-phenyl-5,6-dihydro-2H-pyran-2-one;SCHEMBL979154;3-phenyl-5,6-dihydro-2-pyrone;CXBOBBRQOWTQNB-UHFFFAOYSA-N;DTXSID801293440;5,6-Dihydro-3-phenylpyran-2-one;3-phenyl-5,6-dihydro-pyran-2-one;DB-427124

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-phenyl-5,6-dihydro-2H-pyran-2-one

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:174.068079557
Heavy Atom Count:13
Complexity:224

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COC(=O)C(=C1)C2=CC=CC=C2

Technology Process of 3-phenyl-5,6-dihydro-2H-pyran-2-one

There total 10 articles about 3-phenyl-5,6-dihydro-2H-pyran-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 64.0%

: C₂₃H₂₁O₅P

: 13019-35-7
3-phenyl-5,6-dihydro-2H-pyran-2-one

Guidance literature:: With 2,4,6-trimethyl-pyridine; sodium hexafluoroantimonate; Graphite; In acetonitrile; at 20 ℃; Electrochemical reaction; Inert atmosphere;
DOI:10.1038/s41557-021-00640-2

Reference yield: 50.0%

: C₁₁H₁₁ClO₂

: 13019-35-7
3-phenyl-5,6-dihydro-2H-pyran-2-one

: (R)-3-phenyltetrahydro-2H-pyran-2-one

Guidance literature:: With ketoreductase KRED-P₂B₀₂; nicotinamide adenine dinucleotide phosphate; In aq. phosphate buffer; isopropyl alcohol; for 12h; pH=6.5; enantioselective reaction; Irradiation; Enzymatic reaction;
DOI:10.1038/nature20569

Reference yield:

: 201230-82-2
carbon monoxide

: 192064-78-1
(Z)-4-iodo-4-phenyl-3-buten-1-ol

: 13019-35-7
3-phenyl-5,6-dihydro-2H-pyran-2-one

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; triethylamine; In N,N-dimethyl-formamide; at 100 ℃; for 12h; under 30400 Torr;
DOI:10.3987/com-99-s138