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ChemicalBook--->CAS DataBase List--->1073-05-8

1073-05-8

1073-05-8 Structure

1073-05-8 Structure
IdentificationBack Directory
[Name]

1,3,2-DIOXATHIANE 2,2-DIOXIDE
[CAS]

1073-05-8
[Synonyms]

NSC 526595
trimethylenesulfate
TRIMETHYLENESULPHATE
1,3-Propylenesulfate
Trimethylene sulfate
1,3-Propylene sulfate
1,3-PROPYLENESULPHATE
Propano-1,3-diyl sulfate
1,3-PROPYLENE SULFATE,98%
1,3,2-dioxathiane-2,2-dione
1,3,2-DIOXATHIANE 2,2-DIOXIDE
1,3-PROPANEDIOL CYCLIC SULFATE
1,3,2-Dioxathiane2,2-Dioxide>
1,3-Propanediol, cyclic sulphate
1,3-Propanediol cyclic sulfate 98%
1,3-Propanediol cyclic sulfate,1,3,2-Dioxathiane 2,2-dioxide
[EINECS(EC#)]

214-022-5
[Molecular Formula]

C3H6O4S
[MDL Number]

MFCD00801144
[MOL File]

1073-05-8.mol
[Molecular Weight]

138.14
Chemical PropertiesBack Directory
[Melting point ]

58-62 °C(lit.)
[Boiling point ]

153℃ (14 Torr)
[density ]

1.332 (estimate)
[vapor pressure ]

10Pa at 20℃
[refractive index ]

1.5500 (estimate)
[solubility ]

soluble in No data available
[form ]

solid
[InChI]

InChI=1S/C3H6O4S/c4-8(5)6-2-1-3-7-8/h1-3H2
[InChIKey]

OQYOVYWFXHQYOP-UHFFFAOYSA-N
[SMILES]

O1CCCOS1(=O)=O
[LogP]

0.06 at 20℃
[EPA Substance Registry System]

1,3,2-Dioxathiane, 2,2-dioxide (1073-05-8)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

40
[Safety Statements ]

22-36
[WGK Germany ]

3
[RTECS ]

TY4560000
[HS Code ]

2920901090
Hazard InformationBack Directory
[Uses]

1,3,2-Dioxathiane 2,2-Dioxide is a reagent used in the synthesis of deoxy salacinols via coupling reaction.
[General Description]

Bacillus sp. CCZU11-1 catalyzed biotransformation of 1,3-propanediol cyclic sulfate (1,3-PDS) and its derivatives has been proposed. It can undergo biocatalyzed transformation to diols by Rhodococcus sp.
[Flammability and Explosibility]

Notclassified
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