943-78-2

Basic information

• Product Name: (hexylsulfanyl)benzene
• Synonyms: (Hexylsulfanyl)benzene; benzene, (hexylthio)-; Hexyl phenyl sulfide
• CAS NO: 943-78-2
• Molecular Formula: C₁₂H₁₈S
• Molecular Weight: 194.3363
• Mol File: 943-78-2.mol
• Article Data: 36

Chemical Properties

• Boiling Point: 278.105°C at 760 mmHg
• Flash Point: 118.913°C
• Density: 0.958g/cm³
• Vapor Pressure: 0.007mmHg at 25°C
• Refractive Index: 1.529
• CAS DataBase Reference: (hexylsulfanyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (hexylsulfanyl)benzene(943-78-2)
• EPA Substance Registry System: (hexylsulfanyl)benzene(943-78-2)

Safety Data

• Hazardous Substances Data: 943-78-2(Hazardous Substances Data)

Upstream product

• 109-72-8 n-butyllithium 
• 60-29-7 diethyl ether 
• 622-20-8 1,2-bis(phenylthio)ethane 
• 111-25-1 1-bromo-hexane 
• 108-98-5 thiophenol 
• 1822-73-7 phenylthioethylene 
• 938-10-3 phenylsulfonyl azide 
• 592-41-6 1-hexene 
• 16823-63-5 phenyl hexyl sulfone 
• 75-15-0 carbon disulfide 
• 3111-52-2 potassium thiophenolate 
• 4551-15-9 phenylthiotrimethylsilane 
• 591-50-4 iodobenzene 
• 111-31-9 Hexanethiol 

Downstream Products

• 16823-63-5 phenyl hexyl sulfone 
• 117939-92-1 n-hexyl phenyl sulfoxide 
• 65094-82-8 S-(n-hexyl)-S-phenyl-N-(p-tolylsulfonyl)sulfimide 
• 96001-75-1 2-[3-(4-hexylsulfanyl-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one 
• 91787-21-2 (1-Benzenesulfonyl-hexyl)-trimethyl-silane 
• 106-70-7 methyl hexanoate 
• 124946-51-6 hexylbenzyl selenide 
• 17675-89-7 1-hexaneselenol 
• 139-66-2 diphenyl sulfide 
• 52056-08-3 di-n-hexyl diselenide 
• 94296-11-4 3-chloro-1-(4-(hexylthio)phenyl)propan-1-one 

Relevant articles and documents

Catalytic Reductive Cleavage of Poly(phenylene sulfide) Using a Hydrosilane

The solvent-insoluble poly(phenylene sulfide) main chain was reductively cleaved by using triethylsilane as a hydrogen source under palladium/I c Hex catalytic conditions. After the reaction, benzene and bis(triethylsilyl) sulfide as a sulfide source were formed efficiently. This method could be operated on a gram scale.

Surfactant-Type Catalyst for Aerobic Oxidative Coupling of Hydrazine with Thiol in Water

A series of PEG-functionalized nitrogen ligands were developed to conduct an aerobic oxidative cross-coupling reaction between alkyl- or aryl-hydrazines with thiols in water. This surfactant-type catalyst enables high efficiencies and selectivities, while tolerating a large variety of functional groups. The mother liquor is still catalytically active after five runs.

Synergetic Effect of Monomer Functional Group Coordination in Catalytic Insertion Polymerization

PhS- and PhNH-functionalized dienes are copolymerized efficiently with butadiene to stereoregular copolymers by [(mesitylene)Ni(allyl)][BArF4] (Ni-1). Overall polymerization rates and comonomer incorporations depend strongly on the l