N,N-Dicyclohexyl-2-benzothiazolsulfene amide

CAS: 4979-32-2

Ref. 3D-FD44040

Product Information

• Name: N,N-Dicyclohexyl-2-benzothiazolsulfene amide
• Synonyms: DCBS, 2-Benzothiazolesulfenamide, N,N-dicyclohexyl-, 2-Benzothiazolyl-N,N-dicyclohexylsulfenamide, Accel DZ-G, Accelerator DZ, Accelerator Dcbs, Accelerator Dcbs(Dz), AcceleratorDZ, Cbi-Bb Zero/001988, Dcbs, M 181, Meramid DCH, Mercure DCBS, N,N-Dicyclohexyl-2-Benzothiazole Sulphenamide, N,N-Dicyclohexyl-2-Benzothiazole sulfenamide, N,N-Dicyclohexyl-2-Benzothiazolesulfenamide, N,N-Dicyclohexyl-2-benzothiazolylsulfenamide, N,N-Dicyclohexyl-2-mercaptobenzothiazole sulfenamide, N,N-Dicyclohexylbenzothiazole-2-sulfenamide, N,N-dicyclohexyl-1,3-benzothiazole-2-sulfonamide, N-(1,3-benzothiazol-2-ylsulfanyl)-N-cyclohexylcyclohexanamine, Nocceler DZ, Nocceler DZ-G, Rhodifax 30, Rubber Accelerator DCBS, Rubber Accelerator DZ, SA-DTs, Sanceler DZ, Sanceler DZ-G, Santocure DCBS, Santocure(R) Dcbs, Soxinol DZ, Sulfenamide DTs, Vulkacit DZ

Description

2-Benzothiazolylsulfenamide is a heterocyclic amine that is used as a chemical intermediate. It reacts with hydrochloric acid to produce the corresponding dicyclohexyl amide, which then reacts with ammonia in the presence of an organic base to produce N,N-dicyclohexyl-2-benzothiazolsulfene amide. This reaction mechanism can be summarized as follows:

This compound is not classified as a carcinogen because it does not have significant genotoxic or mutagenic potential. 2-Benzothiazolylsulfenamide has been shown to be an effective crosslinker and additive for plastics, rubber, and textiles.

• Brand: Biosynth

Chemical properties

• Molecular weight: 346.56 g/mol
• Formula: C₁₉H₂₆N₂S₂
• Purity: Min. 95%
• Color/Form: Powder
• InChI: InChI=1S/C19H26N2S2/c1-3-9-15(10-4-1)21(16-11-5-2-6-12-16)23-19-20-17-13-7-8-14-18(17)22-19/h7-8,13-16H,1-6,9-12H2
• InChI key: InChIKey=CMAUJSNXENPPOF-UHFFFAOYSA-N
• SMILES: c1ccc2sc(SN(C3CCCCC3)C3CCCCC3)nc2c1