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1633-83-6 | 1,2-Oxathiane, 2,2-dioxide
CAS No: 1633-83-6 Catalog No: AG001U0A MDL No:MFCD00006584
Product Description
Catalog Number:
AG001U0A
Chemical Name:
1,2-Oxathiane, 2,2-dioxide
CAS Number:
1633-83-6
Molecular Formula:
C4H8O3S
Molecular Weight:
136.1695
MDL Number:
MFCD00006584
IUPAC Name:
oxathiane 2,2-dioxide
InChI:
InChI=1S/C4H8O3S/c5-8(6)4-2-1-3-7-8/h1-4H2
InChI Key:
MHYFEEDKONKGEB-UHFFFAOYSA-N
SMILES:
O=S1(=O)CCCCO1
EC Number:
216-647-9
UNII:
4E0C1CLI2C
NSC Number:
71999
Properties
Complexity:
153
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
136.019g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
136.165g/mol
Monoisotopic Mass:
136.019g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
51.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1
Literature
| Title | Journal |
|---|---|
| Silica-supported sulfonic acid-functionalized ionic liquid coated with [bmim][PF6] as a scavenger for the synthesis of amides. | Molecular diversity 20110201 |
| A novel supramolecular organogel nanotubular template approach for conducting nanomaterials. | The journal of physical chemistry. B 20100121 |
| Self-assembled cylindrical and vesicular molecular templates for polyaniline nanofibers and nanotapes. | The journal of physical chemistry. B 20090827 |
| Masked imidazolyl-dipyrromethanes in the synthesis of imidazole-substituted porphyrins. | The Journal of organic chemistry 20061110 |
| Quantitative structure-activity relationship modeling of acute toxicity of quaternary alkylammonium sulfobetaines to Daphnia magna. | Environmental toxicology and chemistry 20040901 |
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