ChemicalBook Product Catalog Chemical Reagents Organic reagents Sulfone, sulfoxide compound Allyl phenyl sulfone

Allyl phenyl sulfone

Allyl phenyl sulfone Basic information
Product Name:Allyl phenyl sulfone
Synonyms:ALLYL PHENYL SULFONE;ALLYL PHENYL SULPHONE;ALLYLSULFONYLBENZENE;(allylsulphonyl)benzene;Allyl Phenyl sulone;sulfone, allyl phenyl;3-(Phenylsulfonyl)-1-propene;Phenyl (2-propenyl) sulfone
CAS:16212-05-8
MF:C9H10O2S
MW:182.24
EINECS:240-338-8
Product Categories:Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds;Phenyls & Phenyl-Het;Sulfur Compounds (for Synthesis);Synthetic Organic Chemistry;Phenyls & Phenyl-Het;Organic Building Blocks;Sulfones;Sulfur Compounds
Mol File:16212-05-8.mol
Allyl phenyl sulfone Structure
Allyl phenyl sulfone Chemical Properties
Boiling point 110-113 °C/0.5 mmHg (lit.)
density 1.189 g/mL at 25 °C (lit.)
refractive index n20/D 1.548(lit.)
Fp >230 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Orange to Green
Sensitive Light Sensitive
BRN 1863561
InChIKeyKYPIULIVYSQNNT-UHFFFAOYSA-N
CAS DataBase Reference16212-05-8(CAS DataBase Reference)
EPA Substance Registry SystemBenzene, (2-propenylsulfonyl)- (16212-05-8)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
RTECS WR2400000
F 8-10
TSCA T
HazardClass IRRITANT
HS Code 2930909899
Toxicitymouse,LD50,intravenous,320mg/kg (320mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02689,
MSDS Information
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Allyl phenyl sulfone English
SigmaAldrich English
ACROS English
ALFA English
Allyl phenyl sulfone Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS TO FAINTLY YELLOW LIQUID
UsesPossible usages of allyl phenyl sulfone:
  • It can undergo isomerization by the nonionic proazaphosphatrane catalysts under mild reaction conditions.
  • It can react with epoxymesylate to give cycloalkane derivative. This method has been employed in the synthesis of marine eicosanoid bacillariolides I-III.
  • It can undergo electrocatalytic additions to vinyl sulfones catalyzed by an electrogenerated base.
2-[(4-CHLOROPHENYL)SULFONYL]-4-PHENYL-3-BUTENAL O-(2,4-DICHLOROBENZYL)OXIME (4-CHLOROPHENYL)(DIOXO)(3-PHENYL-2-PROPENYL)-LAMBDA6-SULFANE 2-[(4-CHLOROPHENYL)SULFONYL]-4-PHENYL-3-BUTENAL O-METHYLOXIME BIS(P-DIMETHYLAMINOSTYRYL)-P-METHYLPHENYLSULFONYLMETHANE Tetradifon 2-[(4-CHLOROPHENYL)SULFONYL]-4-PHENYL-3-BUTENAL OXIME PHENYL RESIN 4-PHENYL-2-(PHENYLSULFONYL)-3-BUTENAL OXIME 2-[(4-CHLOROPHENYL)SULFONYL]-N,N-DIMETHYL-4-PHENYL-1,3-BUTADIEN-1-AMINE 4-BROMO-3-(((4-CHLOROPHENYL)SULFONYL)METHYL)-2-METHYL-1-PHENYL-3-PYRAZOLIN-5-ONE 4-PHENYL-2-(PHENYLSULFONYL)-3-BUTENAL O-METHYLOXIME DIOXO(PHENYL)(3-PHENYL-2-PROPENYL)-LAMBDA6-SULFANE PHENYL VALERATE Sodium allylsulfonate 5-(4-CHLOROPHENYL)-2-[(PHENYLSULFONYL)METHYL]-3-(2-PYRIDINYLSULFANYL)-2-CYCLOHEXEN-1-ONE N,N-DIMETHYL-4-PHENYL-2-(PHENYLSULFONYL)-1,3-BUTADIEN-1-AMINE Allyl hexanoate 4-BROMO-2-METHYL-3-(((4-METHYLPHENYL)SULFONYL)METHYL)-1-PHENYL-3-PYRAZOLIN-5-ONE
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