5008-73-1

Basic information

• Product Name: ISOPROPYL N-PROPYL SULFIDE
• Synonyms: 1-(Isopropylsulfanyl)propane;2-methyl-3-thiahexane;Isopropylpropyl sulfide;isopropylpropylsulfide;n-Propyl isopropyl sulfide;propane,1-[(1-methylethyl)thio]-;Propyl isopropyl sulfide;propylisopropylsulfide
• CAS NO: 5008-73-1
• Molecular Formula: C₆H₁₄S
• Molecular Weight: 118.24
• EINECS: 225-686-0
• Mol File: 5008-73-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: -96.69°C (estimate)
• Boiling Point: 132 °C
• Flash Point: 23°C
• Appearance: /liquid (estimate)
• Density: 0.83
• Vapor Pressure: 10.1mmHg at 25°C
• Refractive Index: 1.4430 to 1.4460
• CAS DataBase Reference: ISOPROPYL N-PROPYL SULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ISOPROPYL N-PROPYL SULFIDE(5008-73-1)
• EPA Substance Registry System: ISOPROPYL N-PROPYL SULFIDE(5008-73-1)

Safety Data

• Statements: R10:Flammable.
• Safety Statements: S23:Do not inhale gas/fumes/vapour/spray.; S24/25:Avoid contact with skin and eyes.
• RIDADR: UN 1993 3/PG III
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 5008-73-1(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 3627, 1951 DOI: 10.1021/ja01152a021

InChI:InChI=1/C6H14S/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3

Upstream product

• 187737-37-7 propene 
• 20607-43-6 sodium isopropanethiolate 
• 106-94-5 propyl bromide 
• 74-98-6 propane 
• 107-03-9 1-thiopropane 
• 75-26-3 isopropyl bromide 

Downstream Products

• 103375-97-9 C₁₂H₁₈ClNS*C₆H₃N₃O₇ 
• 103375-99-1 C₁₂H₁₈N₂O₂S*C₆H₃N₃O₇ 
• 103375-98-0 C₁₃H₁₈N₂S*C₆H₃N₃O₇ 
• 10035-10-6 hydrogen bromide 
• 124313-19-5 2-<1-(isopropylthio)propyl>phenol 

Relevant articles and documents

Trifluoromethanesulfonic acid catalyzed electrophilic sulfuration of alkanes (cycloalkanes) with elemental sulfur to dialkyl (dicycloalkyl) sulfides

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EFFET PROMOTEUR DES PHOSPHITES ALIPHATIQUES DANS L'ADDITION PHOTO AMORCEE D'H2S SUR LE PROPYLENE EN SOLUTION. I - ETUDE ANALYTIQUE

Aliphatic phosphites have a promotor effect in the radical addition in solution of H2S to propylene photoinitiated as well by direct H2S irradiation as by added benzophenone irradiation.For this last reaction, the phosphite used being (CH3O)3P, the solvent polarity has no effect on the reaction.When the solvent used is a poor hydrogen donnor in a radical reaction, such as benzene, there is an induction period in the case of the benzophenone photoinitiated reaction performed in the presence of a phosphite.It increases for a given aliphatic phosphite with the phosphite concentration and varies with the aliphatic phosphites structure.Light intensity has nearly no effect on the development of the last reaction.