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Prop-1-ene-1,3-sultone

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Prop-1-ene-1,3-sultone Basic information

Product Name:
Prop-1-ene-1,3-sultone
Synonyms:
  • 5H-1,2-Oxathiole, 2,2-dioxide
  • Prop-1-ene-1,3-sultone
  • 1,3-Propene sultone
  • Prop-1-ene-1,3-sulto
  • 1-Propene1,3-Sultone
  • 5H-oxathiole 2,2-dioxide
  • 1-Propene 1,3-Sultone >
  • Prop-1-ene-1,3-sultone1,3-Propene Sultone
CAS:
21806-61-1
MF:
C3H4O3S
MW:
120.13
EINECS:
606-834-7
Mol File:
21806-61-1.mol
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Prop-1-ene-1,3-sultone Chemical Properties

Melting point:
82-83 °C
Boiling point:
257 °C
Density 
1.508
vapor pressure 
0.008-0.018Pa at 20-25℃
Flash point:
109 °C
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
InChI
InChI=1S/C3H4O3S/c4-7(5)3-1-2-6-7/h1,3H,2H2
InChIKey
KLLQVNFCMHPYGL-UHFFFAOYSA-N
SMILES
O1CC=CS1(=O)=O
LogP
-0.49 at 25℃
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Safety Information

HS Code 
2934.99.9001
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Prop-1-ene-1,3-sultone Usage And Synthesis

Chemical Properties

White solid

Uses

Prop-1-ene-1,3-sultone is a chiral compound that can be used as a photoelectron sensitizer. The anion radical created by protonation or deprotonation of the ionized form of prop-1-ene-1,3-sultone can be used to generate singlet oxygen and hydrogen peroxide, which are able to oxidize organic compounds. This compound is also useful in asymmetric synthesis due to its ability to act as a ligand for transition metal ions, such as Fe2+. It has also been shown to have antioxidant properties and is soluble in both organic solvents and deionized water.

Synthesis

A method for producing a Prop-1-ene-1,3-sultone comprises: a step 1 of chlorinating POCl3 or PCl5 with a compound of the chemical formula 2 to produce a compound of the chemical formula 3; a step 2 of diluting the compound of the chemical formula 3 and bromodan (1,3-Dibromo-5,6-dimethylhydantoin) in dichloroethylene solvent and stirring at 20-30°C for four to eight hours to produce 2-halo-1,3-propan sultone of the chemical formula 4; and a step 3 of adding base in the 2-halo-1,3-propan sultone of the chemical formula 4 and stirring for four to eight hours to produce Prop-1-ene-1,3-sultone.

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