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 
• 137-07-5 2-amino-benzenethiol 
• 98-89-5 Cyclohexanecarboxylic acid 
• 1224508-05-7 N-(2-iodophenyl)cyclohexanecarbothioamide 
• 450408-67-0 4,5-dichloro-2-cyclohexanecarbonyl-2H-pyridazin-3-one 
• 20396-49-0 t-butyl cyclohexanecarboperoxoate 
• 110-83-8 cyclohexene 
• 62-53-3 aniline 
• 108-93-0 cyclohexanol 

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.

Late-Stage Alkylation of N-Containing Heteroarenes Enabled by Homolysis of Alkyl-1,4-dihydropyridines under Blue LED Irradiation

Alkylated heteroarenes are widely found in bioactive molecules and pharmaceuticals. Therefore, there is great interest in developing a chemoselective alkylation of heteroarenes under mild conditions, particularly during a late-stage functionalization step for the purpose of rapid derivatization. Herein, we introduce an efficient visible-light-promoted C-H alkylation of nitrogen-containing heteroarenes by using C4-Alkyl 1,4-dihydropyridines (DHPs) as radical precursors at ambient temperatures. A broad scope of heteroarenes, such as 4-hydroxyquinazoline and its derivatives, including those bearing electron-donating or electron-withdrawing groups, can be successfully alkylated in good yields by using various C4-Alkyl DHPs.

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.