33735-40-9

Basic information

• Product Name: 1,3-Oxathiolane, 2,2-diphenyl-
• CAS NO: 33735-40-9
• Molecular Formula: C15H14OS
• Molecular Weight: 242.342
• Mol File: 33735-40-9.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1,3-Oxathiolane, 2,2-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Oxathiolane, 2,2-diphenyl-(33735-40-9)
• EPA Substance Registry System: 1,3-Oxathiolane, 2,2-diphenyl-(33735-40-9)

Safety Data

• Hazardous Substances Data: 33735-40-9(Hazardous Substances Data)

Upstream product

• 119-61-9 benzophenone 
• 60-24-2 2-hydroxyethanethiol 

Downstream Products

• 786-03-8 benzophenone trimethylene acetal 
• 64287-55-4 4-trifluormethylphenyl vinyl sulfide 
• 16411-16-8 p-chlorophenyl vinyl sulfide 
• 16798-93-9 3-methylphenyl vinyl sulfide 
• 64287-54-3 3-methoxyphenyl(vinyl)sulfane 
• 7297-72-5 2-methylphenyl vinyl sulfide 
• 16411-17-9 (4-methoxyphenyl)(vinyl)sulfane 
• 75599-82-5 m-(trifluoromethyl)-phenyl vinyl sulfide 
• 1822-73-7 phenylthioethylene 
• 64287-53-2 (4-fluorophenyl)(vinyl)sulfane 
• 7282-09-9 bis(ethylthio)diphenylmethane 
• 119-61-9 benzophenone 
• 60-24-2 2-hydroxyethanethiol 
• 50939-54-3 Silver; 2-hydroxy-ethanethiolate 

Relevant articles and documents

Silica gel-supported polyphosphoric acid (PPA/SiO2) as an efficient and reusable catalyst for conversion of carbonyl compounds into oxathioacetals and dithioacetals

A simple and efficient method for the conversion of carbonyl compounds to oxathioacetals and dithioacetals by using polyphosphoric acid supported on silica gel (PPA/SiO2) as an acid catalyst have been developed. PPA/SiO2 is easily re

Facile protection of carbonyl compounds as oxathiolanes and thioacetals promoted by PEG1000-based dicationic acidic ionic liquid as chemoselective and recyclable catalyst

Efficient oxathioacetalization and thioacetalization of carbonyl compounds have been achieved in high yields employing PEG1000-based dicationic acidic ionic liquid as a catalyst. The PEG ionic liquid and toluene have the advantages of both homo

An efficient and mild deprotection of 1,3-oxathiolanes to carbonyl compounds using the superoxide ion

An efficient deprotection of 1,3-oxathiolanes to carbonyl compounds has been achieved under the mild reaction conditions of tetraethylammonium superoxide in an aprotic medium at room temperature.