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)
[storage temp. ]

Store at room temperature
[solubility ]

soluble in No data available
[form ]

solid
[Appearance]

White to off-white 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
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS05,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H317-H318-H341-H351
[Precautionary statements ]

P201-P202-P280-P302+P352-P305+P351+P338-P308+P313
[Hazard Codes ]

Xn
[Risk Statements ]

40
[Safety Statements ]

22-36
[RIDADR ]

UN2811
[WGK Germany ]

3
[RTECS ]

TY4560000
[TSCA ]

TSCA listed
[REACH Registrations]

Active
[HazardClass ]

6.1
[HS Code ]

2920901090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Carc. 2
Eye Dam. 1
Muta. 2
Skin Sens. 1B
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
[Synthesis]

1,2-Diol/1,3-diol (50 mmol, 1.0 eq.) was dissolved in CH2Cl2 (30 mL) and the solution was cooled to 0°C. A solution of SOCl2 (65 mmol, 1.3 eq.) in CH2Cl2 (20 mL) was added via a charging funnel over 1 hr. The reaction mixture was heated to reflux for 1 h
Spectrum DetailBack Directory
[Spectrum Detail]

1,3,2-DIOXATHIANE 2,2-DIOXIDE(1073-05-8)1HNMR
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