3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione

Base Information

Chemical Name:3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione
CAS No.:1000697-64-2
Molecular Formula:C₁₆H₁₄O₃
Molecular Weight:254.285
Hs Code.:
DSSTox Substance ID:DTXSID70704947
Wikidata:Q82637545

Synonyms:1000697-64-2;DTXSID70704947;3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione

Suppliers and Price of 3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:254.094294304
Heavy Atom Count:19
Complexity:464

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=C(C=C(C(=O)O2)CC3=CC=CC=C3)C(=O)C1

Technology Process of 3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione

There total 4 articles about 3-Benzyl-7,8-dihydro-2H-1-benzopyran-2,5(6H)-dione 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: 99.0%

: 5669-19-2
2-Benzyl-2-propenoic acid

: 86396-02-3
2-(phenyl-λ³-iodaneylidene)cyclohexane-1,3-dione

: 1000697-64-2
3-benzyl-7,8-dihydro-2H-chromene-2,5(6H)-dione

Guidance literature:: With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; sodium acetate; at 80 ℃; for 12h; Temperature; Reagent/catalyst; Catalytic behavior; Mechanism; Sealed tube;
DOI:10.1021/acs.orglett.0c02618