116967-63-6

Basic information

• Product Name: 2-(2,5-dimethylphenyl)benzo[d]thiazole
• Synonyms: 2-(2,5-dimethylphenyl)benzo[d]thiazole
• CAS NO: 116967-63-6
• Molecular Weight: 239.341
• Mol File: 116967-63-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(2,5-dimethylphenyl)benzo[d]thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,5-dimethylphenyl)benzo[d]thiazole(116967-63-6)
• EPA Substance Registry System: 2-(2,5-dimethylphenyl)benzo[d]thiazole(116967-63-6)

Safety Data

• Hazardous Substances Data: 116967-63-6(Hazardous Substances Data)

Upstream product

• 615-20-3 2-chlorobenzo[d][1,3]thiazole 
• 85199-06-0 2,5-dimethylphenyl boronic acid 
• 1211-32-1 2-(m-tolyl)benzo[d]thiazole 
• 824-45-3 2,5-dimethylbenzyl chloride 
• 137-07-5 2-amino-benzenethiol 
• 95-16-9 1,3-Benzothiazole 
• 553-94-6 4-bromo-m-xylene 

Downstream Products

• 1436570-69-2 C₂₄H₂₂BNS 
• 1436570-45-4 C₃₃H₃₄BNS 

Relevant articles and documents

Rhodium(III)-Catalyzed ortho -C-H Alkylation of 2-Arylbenzothiazoles and 2-Arylthiazoles with Potassium Alkyltrifluoroborates

A general and efficient Rh(III)-catalyzed ortho-C-H alkylation of 2-arylbenzothizazoles and 2-arylthiazoles with potassium alkyltrifluoroborates has been developed. The present method leads to the construction of a library of alkylated 2-arylbenzothiazole

Formation of azaborines by photoelimination of b,n-heterocyclic compounds

Highly fluorescent π-conjugated polycyclic azaborines can be prepared from B,N-heterocyclic compounds with a BR2-CH2 unit through the elimination of an R-H molecule (see scheme). These clean photoelimination reactions occur both in solution and in polymers doped with the precursors. Copyright

Nickel-catalyzed direct arylation of azoles with aryl bromides

Nickel catalyst systems for the direct C2 arylation of oxazoles and thiazoles have been developed. The catalyst systems are cost-efficient and allow the use of various aryl bromides in the C-H arylation of azoles.