CHEBI:53239 - dibenzothiazol-2-yl disulfide

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ChEBI Name dibenzothiazol-2-yl disulfide
ChEBI ID CHEBI:53239
Definition 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.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C14H8N2S4
Net Charge 0
Average Mass 332.48700
Monoisotopic Mass 331.957
InChI InChI=1S/C14H8N2S4/c1-3-7-11-9(5-1)15-13(17-11)19-20-14-16-10-6-2-4-8-12(10)18-14/h1-8H
InChIKey AFZSMODLJJCVPP-UHFFFAOYSA-N
SMILES S(Sc1nc2ccccc2s1)c1nc2ccccc2s1
Roles Classification
Biological Role(s): allergen
A chemical compound which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing dibenzothiazol-2-yl disulfide (CHEBI:53239) has functional parent 1,3-benzothiazole-2-thiol (CHEBI:34292)
dibenzothiazol-2-yl disulfide (CHEBI:53239) has role allergen (CHEBI:50904)
dibenzothiazol-2-yl disulfide (CHEBI:53239) is a benzothiazoles (CHEBI:37947)
dibenzothiazol-2-yl disulfide (CHEBI:53239) is a organic disulfide (CHEBI:35489)
IUPAC Name
2,2'-dithiobis(1,3-benzothiazole)
Synonyms Sources
2,2'-Benzothiazyl disulfide ChemIDplus
2,2'-Bis(benzothiazolyl) disulfide ChemIDplus
2,2'-Dibenzothiazyl disulfide ChemIDplus
2-Mercaptobenzothiazole disulfide ChemIDplus
Benzothiazole disulfide ChemIDplus
benzothiazolyl disulfide ChemIDplus
benzothiazyl disulfide ChemIDplus
Bis(2-benzothiazolyl) disulfide ChemIDplus
Bis(2-benzothiazyl) disulfide ChemIDplus
Bis(benzothiazolyl) disulfide ChemIDplus
BTS-SBT ChEBI
di(1,3-benzothiazol-2-yl) disulfide ChEBI
Dibenzothiazolyl disulfide ChemIDplus
Dibenzothiazolyl disulphide ChemIDplus
Dibenzothiazyl disulfide ChemIDplus
Dibenzoylthiazyl disulfide ChemIDplus
Thiofide ChemIDplus
Manual Xrefs Databases
CN1827608 Patent
EP0112794 Patent
EP0135102 Patent
EP0392052 Patent
View more database links
Registry Numbers Types Sources
120-78-5 CAS Registry Number NIST Chemistry WebBook
120-78-5 CAS Registry Number ChemIDplus
285796 Beilstein Registry Number Beilstein
285796 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
15023086 PubMed citation Europe PMC
18568896 PubMed citation Europe PMC
Last Modified
16 January 2014