2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96

Base Information

Chemical Name:2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96
CAS No.:1029-96-5
Molecular Formula:C17H12 O S
Molecular Weight:264.348
Hs Code.:2934999090
Mol file:1029-96-5.mol

Synonyms:2,6-Diphenyl-4H-4-Thiopyranone;2,6-Diphenyl-g-thiapyrone;2,6-Diphenylthiopyran-4-one; NSC 139252

Suppliers and Price of 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96

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
2,?6-?Diphenyl-?4H-?thiopyran-?4-?one
100mg
$ 145.00

Sigma-Aldrich
2,6-Diphenyl-4H-thiopyran-4-one 96%
500mg
$ 203.00

Chem-Impex
2,6-Diphenyl-4H-thiopyran-4-one,≥95.5%(HPLC),suitableforHematology&Histology ≥95.5%(HPLC)
500MG
$ 223.64

Total 12 raw suppliers

Chemical Property of 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96

Chemical Property:

Vapor Pressure:2.55E-08mmHg at 25°C
Melting Point:126-130℃
Boiling Point:450.9°Cat760mmHg
Flash Point:259.9°C
PSA：45.31000
Density:1.238g/cm³
LogP:4.44230

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,?6-?Diphenyl-?4H-?thiopyran-?4-?one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

General Description 2,6-Diphenyl-4H-thiopyran-4-one is a heterocyclic compound derived from the oxidation of 2,6-diphenyl-4H-thiopyran, forming a thiopyranone structure with phenyl substituents at the 2- and 6-positions. It is a key product in the oxidation of 4H-chalcogenopyrans, particularly when treated with lead tetraacetate, demonstrating its reactivity and potential utility in synthetic chemistry. Other names for 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96 include 2,6-diphenyl-γ-thiapyrone and NSC 139252.

Technology Process of 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96

There total 13 articles about 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96 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: 91.0%