950-47-0

Basic information

• Product Name: Phenoxathiin 10,10-dioxide
• Synonyms: Phenoxathiin 10,10-dioxide;Phenoxathiine 10,10-dioxide
• CAS NO: 950-47-0
• Molecular Formula: C₁₂H₈O₃S
• Molecular Weight: 232.2551
• Mol File: 950-47-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 413.4°Cat760mmHg
• Flash Point: 203.8°C
• Appearance: /
• Density: 1.418g/cm³
• Vapor Pressure: 1.15E-06mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: Phenoxathiin 10,10-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: Phenoxathiin 10,10-dioxide(950-47-0)
• EPA Substance Registry System: Phenoxathiin 10,10-dioxide(950-47-0)

Safety Data

• Hazardous Substances Data: 950-47-0(Hazardous Substances Data)

Usage

General Description

Phenoxathiin 10,10-dioxide is a compound that belongs to the class of organic sulfur compounds. This chemical is commonly referred to as dioxaphenothiazine and is characterized by its fused six-membered rings containing sulfur and oxygen atoms. It exhibits strong electronic properties due to the presence of oxygen atoms in its structure, making it a useful building block in the synthesis of various pharmaceuticals and materials. Phenoxathiin 10,10-dioxide has been found to possess anti-inflammatory and antifungal properties, making it a potential candidate for drug development. Additionally, its unique structure and electronic properties make it a promising candidate for applications in organic electronics and materials science.

InChI:InChI=1/C12H8O3S/c13-16(14)11-7-3-1-5-9(11)15-10-6-2-4-8-12(10)16/h1-8H

Upstream product

• 262-20-4 phenoxathiine 
• 262-24-8 phenoxatellurine 
• 20912-11-2 2-((2-nitrophenyl)thio)phenol 
• 1121-24-0 ortho-mercaptophenol 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 577-19-5 2-nitrophenyl bromide 

Downstream Products

• 134476-36-1 1-Ethylphenoxathiin 10,10-dioxide 
• 120547-00-4 1-((N-(benzyloxycarbonyl)-L-alanyl)oxy)-9-((methoxycarbonyl)dithio)phenoxathiin 10-oxide 
• 120546-99-8 1-((N-(benzyloxycarbonyl)-L-alanyl)oxy)-9-((methoxycarbonyl)dithio)phenoxathiin 
• 135865-60-0 1-(1,2-Dihydroxyethyl)-phenoxathiin-10,10-dioxide 
• 15038-67-2 2,2'-dihydroxydiphenyl sulfone 
• 14909-76-3 2-Hydroxy-2'-isopropoxy-diphenylsulfon 
• 14909-74-1 2-Hydroxy-2'-ethoxy-diphenylsulfon 
• 14909-73-0 2-Hydroxy-2'-methoxy-diphenylsulfon 
• 105583-03-7 2-nitro-phenoxathiine-10,10-dioxide 

Relevant articles and documents

(n5-Cyclo-penta-dienyl)(n6-phenoxathiin 10,10-dioxide)iron(II) hexa-fluoridophosphate and phenoxathiin 10,10-di-oxide

In the structure of the title complex salt, [Fe(C5H 5)(C12H8O3S)]PF6, the coordinated cyclo-penta-dienyl (Cp) and benzene ring planes are almost parallel, with a hinge angle between the planes of 0.8 (2)°. The hinge angle between the planes of the peripheral (coordinated and uncoordinated) benzene rings in the coordinated phenoxathiin 10,10-dioxide mol-ecule is 169.9 (2)°, and the FeCp moiety is located inside the shallow fold of the heterocycle. The hinge angle between the benzene ring planes in the free heterocycle, C 12H8O3S, is 171.49 (6)°.

Green oxidations. Manganese(II) sulfate aided oxidations of organic compounds by potassium permanganate

The oxidation of arenes and sulfides by potassium permanganate was accomplished in good yields under solvent free and heterogeneous conditions when manganese(II) sulfate is used as a solid support. After extraction of the organic products, the inorganic products can be reoxidized to permanganate. This result is important because it provides an approach to oxidation reactions that is, in theory, infinitely sustainable. Springer-Verlag 2007.

A selective, reversible, competitive inhibitor of monoamine oxidase A containing no nitrogen, with negligible potentiation of tyramine-induced blood pressure rise [6]

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