362604-08-8

Basic information

• Product Name: Benzothiazole, 2-[(4-methylphenyl)ethynyl]-
• CAS NO: 362604-08-8
• Molecular Formula: C16H11NS
• Molecular Weight: 249.336
• Mol File: 362604-08-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzothiazole, 2-[(4-methylphenyl)ethynyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-[(4-methylphenyl)ethynyl]-(362604-08-8)
• EPA Substance Registry System: Benzothiazole, 2-[(4-methylphenyl)ethynyl]-(362604-08-8)

Safety Data

• Hazardous Substances Data: 362604-08-8(Hazardous Substances Data)

Upstream product

• 1123-99-5 2-iodobenzothiazole 
• 766-97-2 4-n-methylphenylacetylene 
• 95-16-9 1,3-Benzothiazole 
• 31638-66-1 (p-tolylethynyl)copper 
• 2516-40-7 2-bromo-1,3-benzothiazole 

Relevant articles and documents

Dehydrogenative and decarboxylative C-H alkynylation of heteroarenes catalyzed by Pd(II)-carbene complex

The direct alkynylation of heteroarenes was accomplished with easily prepared Pd(II) carbene complex (Pd Cat.) by two complementary strategies. Pd Cat. catalysed cross-dehydrogenative coupling of terminal alkynes with heteroarenes was achieved in the firs

Synthesis of internal alkynes through the Pd-catalyzed coupling of heteroaryl halides with terminal alkynes

Sonogashira-type cross-couplings of functionalized heterocyclic halides with terminal alkynes were performed efficiently at room temperature. The heteroaryl halides were easily prepared from the corresponding heterocyclic compounds. The catalytic system tolerated a very broad scope of substrates; oxazoles, thiazoles, and furans participate in this type of reaction for the first time. This reaction provides an efficient method for the direct functionalization of heterocycles. Sonogashira-type cross-coupling of functionalized heterocyclic halides with terminal alkynes are performed efficiently at room temperature. The catalytic system tolerates a very broad scope of substrates; oxazoles, thiazoles, and furans participate in this type of reaction for the first time. The reaction provides an efficient method for the direct functionalization of heterocycles. Copyright