10409-06-0

Basic information

• Product Name: DIPHENYLDISULFONE
• Synonyms: DIPHENYLDISULFONE;Disulfone, diphenyl
• CAS NO: 10409-06-0
• Molecular Formula: C₁₂H₁₀O₄S₂
• Molecular Weight: 282.34
• Mol File: 10409-06-0.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 466.2°Cat760mmHg
• Flash Point: 300.2°C
• Appearance: /
• Density: 1.405g/cm³
• Vapor Pressure: 2.02E-08mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: DIPHENYLDISULFONE(CAS DataBase Reference)
• NIST Chemistry Reference: DIPHENYLDISULFONE(10409-06-0)
• EPA Substance Registry System: DIPHENYLDISULFONE(10409-06-0)

Safety Data

• Hazardous Substances Data: 10409-06-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 31, p. 3418, 1966 DOI: 10.1021/jo01348a514Tetrahedron Letters, 36, p. 3849, 1995 DOI: 10.1016/0040-4039(95)00653-T

InChI:InChI=1/C12H10O4S2/c13-17(14,11-7-3-1-4-8-11)18(15,16)12-9-5-2-6-10-12/h1-10H

Upstream product

• 93-59-4 Perbenzoic acid 
• 67-66-3 chloroform 
• 14758-47-5 tetrathioorthocarbonic acid tetraphenyl ester 
• 60-29-7 diethyl ether 
• 140-89-6 potassium ethyl xanthogenate 
• 98-09-9 benzenesulfonyl chloride 
• 618-41-7 Benzenesulfinic acid 
• 6272-36-2 1,2-bis(benzenesulfonyl)hydrazine 
• 599-71-3 piloty's acid 
• 882-33-7 diphenyldisulfane 
• 94-36-0 dibenzoyl peroxide 
• 7732-18-5 water 
• 151-50-8 potassium cyanide 
• 67-64-1 acetone 

Downstream Products

• 882-33-7 diphenyldisulfane 
• 98-10-2 benzenesulfonamide 

Relevant articles and documents

Electrochemical oxidation of sulfinic acids: Efficient oxidative synthesis of diaryl disulfones

Electrochemical oxidation of sulfinic acids has been studied in aqueous solutions using cyclic voltammetry, controlled-potential coulometry, chronoamperometry and chronocoulometry methods. The results indicate that the oxidation of sulfinic acids is an ir

-

-

-

-

Tunable and Practical Synthesis of Thiosulfonates and Disulfides from Sulfonyl Chlorides in the Presence of Tetrabutylammonium Iodide

A tunable and practical synthesis of electrophilic sulfenylating reagents, thiosulfonates and disulfides, from inexpensive and easily available sulfonyl chlorides, has been developed. By appropriate choice of solvents, the reaction of sulfonyl chlorides and tetrabutylammonium iodide gave the target products in good to excellent yields, respectively. These transformations probably proceed through a reducing–coupling pathway. (Figure presented.).

Synthesis of 1,1-difluoroethylsilanes and their application for the introduction of the 1,1-difluoroethyl group

1,1-Difluoroethysilanes (R3SiCF2CH3, R = Me or Et) were synthesized from 1,1-difluoroethyl phenyl sulfone and chlorosilanes using magnesium metal via reductive 1,1-difluoroethylation. It was confirmed that 1,1-difluoroethylsilanes were effective 1,1-difluoroethylating reagents for carbonyl compounds.