3,5-Dimethyl-2h-furo[2,3-c]pyran-2-one

Base Information

Chemical Name:3,5-Dimethyl-2h-furo[2,3-c]pyran-2-one
CAS No.:857054-07-0
Molecular Formula:C₉H₈O₃
Molecular Weight:164.161
Hs Code.:
DSSTox Substance ID:DTXSID401296628
Nikkaji Number:J2.454.597K
Mol file:857054-07-0.mol

Synonyms:857054-07-0;3,5-Dimethyl 2H-Furo[2,3-c]pyran-2-one;3,5-dimethyl-2h-furo[2,3-c]pyran-2-one;3,5-dimethylfuro[2,3-c]pyran-2-one;3,4-Dimethyl 2H-Furo[2,3-c]pyran-2-one;SCHEMBL3849796;DTXSID401296628;FT-0667447

Suppliers and Price of 3,5-Dimethyl-2h-furo[2,3-c]pyran-2-one

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
Packaging
price

TRC
3,5-Dimethyl2H-Furo[2,3-c]pyran-2-one
25mg
$ 1230.00

Total 2 raw suppliers

Chemical Property of 3,5-Dimethyl-2h-furo[2,3-c]pyran-2-one

Chemical Property:

PSA：43.35000
LogP:1.95440
XLogP3:0.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:164.047344113
Heavy Atom Count:12
Complexity:345

Purity/Quality:

98% ^*data from raw suppliers

3,5-Dimethyl2H-Furo[2,3-c]pyran-2-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C(=O)OC2=CO1)C
Uses KAR3 is a compound in smoke responsible for promoting the seed germination of a wide range of plant species. smoke. KAR3 is a compound in smoke responsible for promoting the seed germination of a wide range of plant species. The researchers named the compounds “the karrikins”, for “karrik”, an aboriginal word for smoke.

Technology Process of 3,5-Dimethyl-2h-furo[2,3-c]pyran-2-one

There total 4 articles about 3,5-Dimethyl-2h-furo[2,3-c]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:

: 644-46-2
allomaltol

: 857054-07-0
3,5-dimethyl-2H-furo[2,3-c]pyran-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: P₂S₅; NaHCO₃ / tetrahydrofuran / 3 h / 20 °C

2: Et₃N / CH₂Cl₂ / 0.17 h / 0 °C

3: 57.4 mg / NaOAc; PPh₃; Ac₂O / 0.5 h / Heating

With tetraphosphorus decasulfide; sodium acetate; acetic anhydride; sodium hydrogencarbonate; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jf0633241

Reference yield:

: 30717-77-2
5-hydroxy-2-methyl-thiopyran-4(1H)-one

: 857054-07-0
3,5-dimethyl-2H-furo[2,3-c]pyran-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0.17 h / 0 °C

2: 57.4 mg / NaOAc; PPh₃; Ac₂O / 0.5 h / Heating

With sodium acetate; acetic anhydride; triethylamine; triphenylphosphine; In dichloromethane;
DOI:10.1021/jf0633241