15848-07-4

Basic information

• Product Name: Methanethione, diphenyl-, S-oxide
• Synonyms: FNNSWZAKAFPQOO-UHFFFAOYSA;thiobenzophenone S-oxide;Methanethione,diphenyl-,S-oxide;diphenyl-sulfinyl-methane;diphenyl-methanethione S-oxide;InChI=1/C13H10OS/c14-15-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
• CAS NO: 15848-07-4
• Molecular Formula: C13H10OS
• Molecular Weight: 214.288
• Mol File: 15848-07-4.mol
• Article Data: 8

Chemical Properties

• Melting Point: 30-32 °C (decomp)(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
• Boiling Point: 332.6±25.0 °C(Predicted)
• Density: 1.08±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Methanethione, diphenyl-, S-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: Methanethione, diphenyl-, S-oxide(15848-07-4)
• EPA Substance Registry System: Methanethione, diphenyl-, S-oxide(15848-07-4)

Safety Data

• Hazardous Substances Data: 15848-07-4(Hazardous Substances Data)

Upstream product

• 132102-75-1 4,4'-diphenylmethyl (phenylsulfonyl)methyl sulfoxide 
• 1450-31-3 Thiobenzophenon 
• 109649-63-0 diphenyl-methanethiosulfonic acid S-benzyl ester 
• 106864-86-2 methyl diphenylmethanesulfinate 
• 132102-78-4 diphenylmethyl <(p-methoxyphenyl)sulfonyl>methyl sulfoxide 
• 132102-76-2 diphenylmethyl <(p-chlorophenyl)sulfonyl>methyl sulfoxide 
• 132102-77-3 diphenylmethyl (p-tolylsulfonyl)methyl sulfoxide 

Downstream Products

• 60870-95-3 2,2-diphenyloxathiirane 
• 65159-44-6 1-(4-nitrophenyl)-2,2-diphenylethanone 
• 34519-98-7 1,1,2-Triphenylethyl-benzylsulfid 
• 58-72-0 Triphenylethylene 
• 1450-31-3 Thiobenzophenon 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 119-61-9 benzophenone 
• 16911-57-2 thiobenzoic acid O-phenyl ester 
• 884-09-3 phenyl thiobenzoate 
• 97745-99-8 C₃₃H₂₃NOS 
• 80423-95-6 C₁₆H₁₈OS 
• 80413-62-3 C₂₁H₂₈S 
• 101-81-5 Diphenylmethane 
• 80413-63-4 C₁₇H₂₀OS 

Relevant articles and documents

Regioselective 1,3-dipolar cycloadditions of a 'thiocarbonyl-methanide' ((alkylidenesalfonio)methanide) with aromatic sulfines

Reaction of the spirocyclic 2,5-dihydro-1,3,4-thiadiazole 7 and thiobenzophenone S-oxide (6a) in THF at 45° yielded the spirocyclic 1,3-dithiolane 1-oxide 8, thiirane 9, and the diazane derivative 10 in a ratio of 61:15:23 (Scheme 2) The formation of 8 is

A convenient preparation of sulfines (R2C=S=O) from thioketones

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Matrix isolation of diphenylsulfene and diphenyl-α-sultine

Diphenylsulfene (5) and diphenyl-α-sultine 6 were generated in cryogenic matrices by three independent routes: (i) the thermal reaction of diphenylcarbene (8) and SO2, (ii) the photochemically induced hetero Wolff rearrangement of sulfonylcarbe