16215-14-8

Basic information

• Product Name: 3-(Methylsulphonyl)-1-propene
• Synonyms: 3-(Methylsulphonyl)-1-propene;Allyl(methyl) sulfone;Allyl(methyl)sulfone;Allylmethyl sulfone;1-Propene,3-(Methylsulfonyl);3-(Methylsulfonyl)-1-propene;Allyl methyl sulfone 96%;3-methylsulfonylprop-1-ene
• CAS NO: 16215-14-8
• Molecular Formula: C₄H₈O₂S
• Molecular Weight: 120.17
• Product Categories: Allyl Monomers;Alternative Energy;Battery Electrolyte Materials;Electrolytes;Lithium-Ion Batteries;Materials Science;Monomers;Polymer Science;Solvents
• Mol File: 16215-14-8.mol
• Article Data: 30

Chemical Properties

• Melting Point: 87-88 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 230.86°C (estimate)
• Flash Point: >110°C
• Appearance: /
• Density: 1.171g/mLat 25℃
• Vapor Pressure: 0.0477mmHg at 25°C
• Refractive Index: n20/D 1.472
• CAS DataBase Reference: 3-(Methylsulphonyl)-1-propene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Methylsulphonyl)-1-propene(16215-14-8)
• EPA Substance Registry System: 3-(Methylsulphonyl)-1-propene(16215-14-8)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• WGK Germany: 3
• Hazardous Substances Data: 16215-14-8(Hazardous Substances Data)

Usage

General Description

This product has been enhanced for energy efficiency.

InChI:InChI=1/C4H8O2S/c1-3-4-7(2,5)6/h3H,1,4H2,2H3

Upstream product

• 10152-76-8 allylmethyl sulfide 
• 21892-75-1 allylmethylsulfoxide 
• 24850-33-7 allyltributylstanane 
• 74-88-4 methyl iodide 
• 723336-87-6 trimethylsilyl prop-2-ene-1-sulfinate 
• 77-78-1 dimethyl sulfate 
• 54533-11-8 1-chloro-3-(methanesulfonyl)propane 
• 106-95-6 allyl bromide 
• 124-63-0 methanesulfonyl chloride 
• 107-05-1 3-chloroprop-1-ene 
• 107268-47-3 (+/-)-3β-acetoxy-1-methylsulphonyloxymethyltropane 
• 1730-25-2 allylmagnesium bromide 
• 5296-64-0 allyl phenyl thioether 
• 762-72-1 allyl-trimethyl-silane 

Downstream Products

• 6943-88-0 1-methanesulfonyl-propane-2-sulfonic acid ; sodium-salt 
• 122156-03-0 (Z)‐1‐(prop‐2‐enyldisulfanyl)prop‐1‐en 
• 122156-03-0 (E)-1-allyl-2-(prop-1-en-1-yl) disulfane 
• 75-07-0 acetaldehyde 
• 1260118-90-8 1-(4-(3-(methylsulfonyl)propyl)phenyl)ethanone 
• 1448510-40-4 S-{[1,7-di(diphenylamino)-1,7-dioxo]heptan}-4-yl O-ethyl carbonodithioate 
• 1448510-41-5 S-[1,7-di(methanesulfonylphenylamino)-1,7-dioxoheptan]-4-yl O-ethyl carbonodithioate 
• 1448510-33-5 S-(1,7-dioxo-1,7-diphenylheptan)-4-yl O-ethyl carbonodithioate 
• 1448510-38-0 S-(1,7-dioxo-1,7-diphenoxyheptan)-4-yl O-ethyl carbonodithioate 
• 1465082-79-4 S-[1,7-di(4-chlorophenoxy)-1,7-dioxoheptan]-4-yl O-ethyl carbonodithioate 
• 1465082-81-8 S-[1,7-di(4-nitrophenoxy)-1,7-dioxoheptan]-4-yl O-ethyl carbonodithioate 
• 1448510-39-1 S-(1,7-dibenzyloxy-1,7-dioxoheptan)-4-yl O-ethyl carbonodithioate 
• 1448510-34-6 S-[1,7-dioxo-1,7-di(4-methoxyphenyl)heptan]-4-yl O-ethyl carbonodithioate 
• 955085-06-0 1,4-dimethylsulphonyl-2-butene 

Relevant articles and documents

Air atmospheric photocatalytic oxidation by ultrathin C,N-TiO2nanosheets

Herein, we demonstrate the highly efficient photocatalytic sulfide oxidation reaction under mild conditions,i.e.in air, at room temperature and in the absence of a sacrificial reagent, co-catalyst or redox mediator, by using ultrathin C,N-TiO2nanosheets as a photocatalyst.

Electrolyte for rechargeable lithium battery and rechargeable lithium battery

An electrolyte for a rechargeable lithium battery and a rechargeable lithium battery including the electrolyte, the electrolyte including a non-aqueous organic solvent; a lithium salt; and an additive, wherein the additive includes a compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, R is a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C1 to C10 alkoxy group, a substituted or unsubstituted C2 to C10 alkenyl group, a substituted or unsubstituted C2 to C10 alkynyl group, a substituted or unsubstituted C3 to C10 cycloalkyl group, a substituted or unsubstituted C3 to C10 cycloalkenyl group, or a substituted or unsubstituted C6 to C20 aryl group, and n is an integer of 1 to 3.

Synthesis of Na22[((RE)4(H2O)6Sb6O4)(SbW10O37)2(SbW8O31)2] [(RE)III = Y, Gd, Tb, Dy, Ho, Er, Tm, Yb]: Synthesis, characterization and catalytic application

A series of eight rare-earth substituted antimony tungstates with the formulae [((RE)4(H2O)6Sb6O4)(SbW10O37)2(SbW8O31)2]22– [(RE)III = Y(1), Gd(2), Tb(3), Dy(4), Ho(5), Er(6), Tm(7), Yb(8)] has been synthesized under ambient conditions. The compounds were isolated using rare-earth salts and Na9[B-α-SbW9O33]?19.5 H2O as precursors along with sodium dihydrogen phosphate in 1 M NaCl solution. The addition of dihydrogen phosphate was found to be a crucial step for the isolation of these polyanions. The polyanions were characterized by various analytical techniques such as single crystal X-ray diffraction (1a – 6a) (SC-XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA). The compounds were found to show efficient heterogeneous catalytic activity for oxidation of thioethers.