2(5H)-Furanone, 3-(phenylsulfinyl)-

Base Information

Chemical Name:2(5H)-Furanone, 3-(phenylsulfinyl)-
CAS No.:57061-31-1
Molecular Formula:C10H8O3S
Molecular Weight:208.238
Hs Code.:
DSSTox Substance ID:DTXSID50451285
Nikkaji Number:J270.739J

Synonyms:3-(phenylsulfinyl)-2(5H)-furanone;2(5H)-Furanone, 3-(phenylsulfinyl)-;57061-31-1;3-(benzenesulfinyl)-5H-furan-2-one;DTXSID50451285

Suppliers and Price of 2(5H)-Furanone, 3-(phenylsulfinyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2(5H)-Furanone, 3-(phenylsulfinyl)-

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:208.01941529
Heavy Atom Count:14
Complexity:290

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C=C(C(=O)O1)S(=O)C2=CC=CC=C2

Technology Process of 2(5H)-Furanone, 3-(phenylsulfinyl)-

There total 5 articles about 2(5H)-Furanone, 3-(phenylsulfinyl)- 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: 73.0%

: 42435-82-5
3-Phenylsulfanylfuran-2(5H)-one

: 57061-31-1
3-benzenesulfinyl-5H-furan-2-one

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid;
DOI:10.1080/00397919608003719

Reference yield:

: 35998-30-2
3-(phenylsulfanyl)-3,4-dihydrofuran-2-one

: 57061-31-1
3-benzenesulfinyl-5H-furan-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / SO₂Cl₂ / CCl₄ / 2 h / 0 °C

2: 65 percent / LiBr, Li₂CO₃ / tetrahydrofuran / 0.5 h / Heating

3: 73 percent / MCPBA / CH₂Cl₂ / 1 h / -15 °C

With sulfuryl dichloride; lithium carbonate; 3-chloro-benzenecarboperoxoic acid; lithium bromide; In tetrahydrofuran; tetrachloromethane; dichloromethane;
DOI:10.1039/p19960001913

Reference yield:

: 62675-47-2
α-chloro-α-(phenylthio)-γ-butyrolactone

: 57061-31-1
3-benzenesulfinyl-5H-furan-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / LiBr, Li₂CO₃ / tetrahydrofuran / 0.5 h / Heating

2: 73 percent / MCPBA / CH₂Cl₂ / 1 h / -15 °C

With lithium carbonate; 3-chloro-benzenecarboperoxoic acid; lithium bromide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/p19960001913