4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-

Base Information

Chemical Name:4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-
CAS No.:60839-95-4
Molecular Formula:C17H14OS
Molecular Weight:266.364
Hs Code.:
DSSTox Substance ID:DTXSID00485414
Nikkaji Number:J2.332.052E

Synonyms:4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-;60839-95-4;2,6-diphenyl-4-thiapyrone;DTXSID00485414;SVCXGQAZLQTSIR-UHFFFAOYSA-N;2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one

Suppliers and Price of 4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-

Supply Marketing:

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

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Chemical Property of 4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:266.07653624
Heavy Atom Count:19
Complexity:348

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(SC(=CC1=O)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl-

There total 7 articles about 4H-Thiopyran-4-one, 2,3-dihydro-2,6-diphenyl- 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: 94.0%

: 37845-36-6
(E)-1,5-diphenyl-1-penten-4-yn-3-one

: 60839-95-4
2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one

Guidance literature:: With sodium hydrogensulfide; In 2-methoxy-ethanol; at 40 ℃;
DOI:10.1016/j.tetlet.2006.05.080

Reference yield:

: 63124-66-3,128812-14-6
(1E)-1,5-diphenylpent-1-en-4-yn-3-ol

: 60839-95-4
2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / MnO₂ / CH₂Cl₂ / 23 °C

2: 94 percent / Na₂S*9H₂O / tetrahydrofuran; H₂O / 72 h / 23 °C

With manganese(IV) oxide; sodium sulfide; In tetrahydrofuran; dichloromethane; water; 2: thia-Michael reaction;
DOI:10.1007/s00706-006-0571-4

Reference yield:

: 536-74-3
phenylacetylene

: 60839-95-4
2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-BuLi / tetrahydrofuran / 1.5 h / -78 °C

1.2: 89 percent / tetrahydrofuran / 1.5 h / -78 °C

2.1: 96 percent / MnO₂ / CH₂Cl₂ / 23 °C

3.1: 94 percent / Na₂S*9H₂O / tetrahydrofuran; H₂O / 72 h / 23 °C

With manganese(IV) oxide; sodium sulfide; n-butyllithium; In tetrahydrofuran; dichloromethane; water; 3.1: thia-Michael reaction;
DOI:10.1007/s00706-006-0571-4