89987-96-2

Basic information

• Product Name: Disulfide, bis(3-phenylpropyl)
• Synonyms: Diphenpropyl disulfide;bis-3-phenylpropyldisulfide
• CAS NO: 89987-96-2
• Molecular Formula: C18H22S2
• Molecular Weight: 302.505
• Mol File: 89987-96-2.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 194-195 °C(Press: 1.5 Torr)
• Density: 1.092±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Disulfide, bis(3-phenylpropyl)(CAS DataBase Reference)
• NIST Chemistry Reference: Disulfide, bis(3-phenylpropyl)(89987-96-2)
• EPA Substance Registry System: Disulfide, bis(3-phenylpropyl)(89987-96-2)

Safety Data

• Hazardous Substances Data: 89987-96-2(Hazardous Substances Data)

Upstream product

• 637-59-2 1-Bromo-3-phenylpropane 
• 79528-83-9 (3-thiocyanatopropyl)benzene 
• 3012-37-1 benzyl thiocyanate 
• 122-97-4 3-Phenyl-1-propanol 
• 24734-68-7 3-Phenylpropane-1-thiol 
• 5799-67-7 dimethyl(methylthio)sulfonium tetrafluoroborate 
• 114764-11-3 3-phenylpropyl 2-(trimethylsilyl)ethyl sulfide 

Downstream Products

• 63014-04-0 3-Phenyl-propane-1-sulfonyl chloride 
• 90220-25-0 3-phenyl-1-propane-sulfonamide 
• 89987-01-9 Tetraisopropyl (3-phenyl-propylthio)-methylene-diphosphonate 
• 22776-35-8 2,3-dihydro-4H-1-benzothiopyran 1,1-dioxide 
• 2054-35-5 thiochromane 
• 24734-68-7 3-Phenylpropane-1-thiol 

Relevant articles and documents

Cu-mediated: vs. Cu-free selective borylation of aryl alkyl sulfones

A Cu-catalysed borylation of aryl alkyl sulfones was developed for the high yield synthesis of versatile arylboronic esters using a readily prepared NHC-Cu catalyst. In addition, the selective cleavage of either alkyl(C)-sulfonyl or aryl(C)-sulfonyl bonds

A rapid, efficient and green procedure for transformation of alkyl halides/ tosylates to organochalcogens in water

A one-pot and efficient synthesis of dialkyl dichalcogenides (S, Se) in aqueous media under catalyst-free conditions using benzylic, allylic and primary halides with elemental sulfur and selenium has been developed. Also, this procedure was extended to preparation of trisulfides and triselenides from secondary and tertiary halides in same condition. In all cases, products can be obtained in good to excellent yield in short reactions time.

Symmetrical disulfide synthesis via nickel-catalysis using potassium sulfide as sulfur source

Abstract: An efficient one-pot method for the synthesis of organic disulfides from aryl and alkyl halides and potassium sulfide has been described. K2S acts as an inexpensive and readily available sulfur source. A variety of symmetric diaryl and dialkyl disulfides was prepared in good to excellent yields using NiCl2·6H2O and acetylacetone as the catalytic system. Graphical abstract: [Figure not available: see fulltext.]