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66304-01-6 | 3H-1,2-Benzodithiol-3-one, 1,1-dioxide
CAS No: 66304-01-6 Catalog No: AG0033PU MDL No:MFCD00132960
Product Description
Catalog Number:
AG0033PU
Chemical Name:
3H-1,2-Benzodithiol-3-one, 1,1-dioxide
CAS Number:
66304-01-6
Molecular Formula:
C7H4O3S2
Molecular Weight:
200.2349
MDL Number:
MFCD00132960
IUPAC Name:
1,1-dioxo-1λ6,2-benzodithiol-3-one
InChI:
InChI=1S/C7H4O3S2/c8-7-5-3-1-2-4-6(5)12(9,10)11-7/h1-4H
InChI Key:
JUDOLRSMWHVKGX-UHFFFAOYSA-N
SMILES:
O=C1SS(=O)(=O)c2c1cccc2
Properties
Complexity:
301
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
199.96g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
200.226g/mol
Monoisotopic Mass:
199.96g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
84.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1
Literature
| Title | Journal |
|---|---|
| Thiol-dependent DNA cleavage by aminomethylated Beaucage's reagent. | Organic & biomolecular chemistry 20100321 |
| Antagonistic interaction between systemic acquired resistance and the abscisic acid-mediated abiotic stress response in Arabidopsis. | The Plant cell 20080601 |
| Solid-phase chemical synthesis of phosphonoacetate and thiophosphonoacetate oligodeoxynucleotides. | Journal of the American Chemical Society 20030129 |
| Inactivation of the human papillomavirus-16 E6 oncoprotein by organic disulfides. | Bioorganic & medicinal chemistry 20001101 |
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