Molecular structure of 2,6-Diphenyl-4H-thiopyran-4-one, CAS Number: 1029-96-5
2,6-Diphenyl-4H-thiopyran-4-one (CAS 1029-96-5)
Application:
2,6-Diphenyl-4H-thiopyran-4-one is a small molecule with cross-conjugated dienones
CAS Number:
1029-96-5
Molecular Weight:
264.34
Molecular Formula:
C17H12OS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Description
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SDS & Certificate of Analysis
This has cross-conjugated dienones with sterically hindered electrophilic beta-carbons, and it does not inhibit isopeptidases or cause significant cell death.
2,6-Diphenyl-4H-thiopyran-4-one (CAS 1029-96-5) References
- Pharmacophore model for novel inhibitors of ubiquitin isopeptidases that induce p53-independent cell death. | Mullally, JE. and Fitzpatrick, FA. 2002. Mol Pharmacol. 62: 351-8. PMID: 12130688
- Photoreaction of 2, 6-Diphenyl-4H-thiopyran-4-one. | Sugiyama, Noboru, et al. 1969. Bulletin of the Chemical Society of Japan. 42.10: 3005-3007.
- The Photoreaction of 2, 6-Diphenyl-4H-thiopyran-4-one and Its Related Compounds. | Sugiyama, Noboru, et al. 1970. Bulletin of the Chemical Society of Japan. 43.10: 3205-3209.
- Photolysis of 2, 6-diphenyl-4h-pyran-4-thione and 2, 6-diphenyl-4h-thiopyran-4-thione. | Ishibe, N., et al. 1973. Tetrahedron. 29.14: 2005-2008.
- Photoreaction of 2, 6-diphenyl-4H-thiopyran-4-one 1, 1-dioxide with arylacetylenes. | Ishibe, Nobuyuki, et al. 1974. The Journal of Organic Chemistry. 39.1: 103-104.
- Stereospecific synthesis of D-threo-sphinganine. | Newman, Howard. 1974. The Journal of Organic Chemistry. 39.1: 100-103.
- The reaction of 2, 6‐diphenyl‐2, 3, 5, 6‐tetrahydro‐4H‐thiopyran‐4‐one with sulfuryl chloride. | Van Allan, J. A., et al. 1977. Journal of Heterocyclic Chemistry. 14.8: 1399-1402.
- Chemistry of 1, 1-dioxothiopyrans. 1. Syntheses and reactions of 2, 6-diphenyl-4H-thiopyran-4-one 1, 1-dioxide and 4H-thioflaven-4-one 1, 1-dioxide. | Chen, Chin H., et al. 1986. The Journal of Organic Chemistry. 51.17: 3282-3289.
- A physical Study on the Aromaticity of 4H-Pyran-4-one, 9H-Xanthen-9-one, and related sulphur Compounds. | Lumbroso, Henri, et al. 1986. Zeitschrift für Naturforschung A. 41.10: 1250-1257.
- Oxidation reactions of 4H-chalcogenopyrans. | Drevko, B. I., et al. 1996. Chemistry of Heterocyclic Compounds. 32: 777-780.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,6-Diphenyl-4H-thiopyran-4-one, 500 mg | sc-214035 | 500 mg | $190.00 |