2,2-Dithiobis (Benzothiazole)

Chemical Information
Dibenzothiazol-2-yl disulfide is an organic disulfide resulting from the formal oxidative coupling of the thiol groups of two molecules of 1,3-benzothiazole-2-thiol. It is used as an accelerator in the rubber industry. It has a role as an allergen. It is an organic disulfide and a member of benzothiazoles. It is functionally related to a 1,3-benzothiazole-2-thiol.
| CAS Number | 120-78-5 |
| PubChem CID | 8447 |
| IUPAC Name | 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole |
| Molecular Formula | C14H8N2S4 |
| Molecular Weight | 332.5 |
| XLogP | 5.6 |
| Topological Polar Surface Area | 133 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 311 |
| Property | Value |
|---|---|
| Molecular Weight | 332.5 |
| XLogP3 | 5.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 331.95703296 |
| Monoisotopic Mass | 331.95703296 |
| Topological Polar Surface Area | 133 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 311 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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