40115-03-5

Basic information

• Product Name: Benzothiazole, 2-cyclohexyl- (9CI)
• Synonyms: Benzothiazole, 2-cyclohexyl- (9CI)
• CAS NO: 40115-03-5
• Molecular Formula: C₁₃H₁₅NS
• Molecular Weight: 217.3299
• Product Categories: BENZOTHIAZOLE
• Mol File: 40115-03-5.mol
• Article Data: 82

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzothiazole, 2-cyclohexyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-cyclohexyl- (9CI)(40115-03-5)
• EPA Substance Registry System: Benzothiazole, 2-cyclohexyl- (9CI)(40115-03-5)

Safety Data

• Hazardous Substances Data: 40115-03-5(Hazardous Substances Data)

Upstream product

• 1123-99-5 2-iodobenzothiazole 
• 24371-94-6 cyclohexylmercury chloride 
• 95-16-9 1,3-Benzothiazole 
• 108-85-0 1-bromocyclohexane 
• 626-62-0 Cyclohexyl iodide 
• 41320-40-5 <<(methylthio)thiocarbonyl>oxy>cyclohexane 
• 1224508-05-7 N-(2-iodophenyl)cyclohexanecarbothioamide 
• 104-94-9 4-methoxy-aniline 
• 137-07-5 2-amino-benzenethiol 
• 2043-61-0 cyclohexanecarbaldehyde 
• 110-82-7 cyclohexane 
• 103-72-0 phenyl isothiocyanate 
• 62-53-3 aniline 
• 126812-30-4 1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate 

Relevant articles and documents

Method for catalytically synthesizing benzothiazole compound by using copper complex

The invention relates to a method for catalytically synthesizing benzothiazole compounds by using a copper complex, which is characterized in that a copper complex containing ortho-carborane Schiff base ligand is used as a catalyst to form aldehydes. 2 - Bromoaniline and sodium sulfide are used as raw materials, and the reaction is carried out at room temperature to obtain a benzothiazole compound. Compared with the prior art, the copper complex catalytic aldehyde, 2 -bromoaniline and sodium sulfide (Na) containing the ortho-carborane Schiff base ligand are utilized. 2 Multiple components of S) react to prepare benzothiazole compounds, and the catalyst is low in dosage, mild in reaction conditions, high in reaction rate, high in yield, wide in substrate range, cheap and accessible in raw materials and wide in application prospect in industry.

Photoelectrochemical cross-dehydrogenative coupling of benzothiazoles with strong aliphatic C-H bonds

A photoelectrochemical strategy for the cross-dehydrogenative coupling of unactivated aliphatic hydrogen donors (e.g.alkanes) with benzothiazoles is reported. We used tetrabutylammonium decatungstate as the photocatalyst to activate strong C(sp3)-H bonds in the chosen substrates, while electrochemistry scavenged the extra electrons.

Visible-Light-Mediated Alkenylation of Alkyl Boronic Acids without an External Lewis Base as an Activator

Herein we report a protocol for the direct visible-light-mediated alkenylation of alkyl boronic acids at room temperature without an external Lewis base as an activator, and we propose a mechanism involving benzenesulfinate activation of the alkyl boronic acids. The protocol permits the efficient functionalization of a broad range of cyclic and acyclic primary and secondary alkyl boronic acids with various alkenyl sulfones. We demonstrated its utility by preparing or functionalizing several pharmaceuticals and natural products.