58749-30-7

Basic information

• Product Name: (3-phenylpropane-1,1-diyl)bis(phenylsulfane)
• Synonyms: (3-phenylpropane-1,1-diyl)bis(phenylsulfane)
• CAS NO: 58749-30-7
• Molecular Weight: 336.522
• Mol File: 58749-30-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (3-phenylpropane-1,1-diyl)bis(phenylsulfane)(CAS DataBase Reference)
• NIST Chemistry Reference: (3-phenylpropane-1,1-diyl)bis(phenylsulfane)(58749-30-7)
• EPA Substance Registry System: (3-phenylpropane-1,1-diyl)bis(phenylsulfane)(58749-30-7)

Safety Data

• Hazardous Substances Data: 58749-30-7(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 3561-67-9 bis(phenylthio)methane 
• 104-53-0 3-phenyl-propionaldehyde 
• 108-98-5 thiophenol 
• 30076-98-3 (3,3-dimethoxypropyl)benzene 

Downstream Products

• 104-53-0 3-phenyl-propionaldehyde 
• 79294-25-0 dimethyl(phenyl)(3-phenylpropyl)silane 
• 1138-44-9 2-phenethylcyclohexanone 
• 78427-96-0 1-phenyloctan-4-one 
• 1567359-99-2 (1E)-1,6-diphenyl-3-(triisopropylsiloxy)-1,3-hexadiene 
• 1567360-00-2 (1E)-1,6-diphenyl-3-(triisopropylsiloxy)-1,3-hexadiene 
• 94404-40-7 C₁₅H₁₅FOS 
• 1060646-10-7 methyl 6-phenyl-2,4,4-tris(phenylthio)hexanoate 
• 167366-75-8 2-methyl-7-phenyl-3,5,5-tris(phenylthio)heptan-2-ol 

Relevant articles and documents

Dimeric Potassium Amide-Catalyzed α-Alkylation of Benzyl Sulfides and 1,3-Dithianes

The first catalytic α-alkylation reaction of benzyl sulfides and 1,3-dithianes with styrenes and conjugated dienes was developed under mild conditions by using a readily available Br?nsted base potassium bis(trimethylsilyl)amide (KHMDS) as catalyst. The reaction displayed good functional group tolerance, high efficiency, and excellent chemoselectivity. A series of desired alkylation products were obtained in good to high yield. Preliminary mechanism studies suggested that two of the potassium amide catalyst molecules worked together in the catalytic cycle.

Pyrylium Salt Sensitized Photochemical Deprotections of Dithioacetals and Ketals

Photoreactions of various dithioacetals and ketals using tris(p-chlorophenyl)pyrylium perchlorate as a sensitizer were studied.Irradiation (λ>360 nm) of dichloromethane solutions containing dithioacetals or ketals and pyrylium salt afforded the corresponding carbonyl compounds in good to excellent yields in the presence of molecular oxygen.