1268700-01-1

Basic information

• Product Name: (5-chlorobenzo[d]thiazol-2-yl)(4-fluorophenyl)methanone
• Synonyms: (5-chlorobenzo[d]thiazol-2-yl)(4-fluorophenyl)methanone
• CAS NO: 1268700-01-1
• Molecular Weight: 291.733
• Mol File: 1268700-01-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (5-chlorobenzo[d]thiazol-2-yl)(4-fluorophenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-chlorobenzo[d]thiazol-2-yl)(4-fluorophenyl)methanone(1268700-01-1)
• EPA Substance Registry System: (5-chlorobenzo[d]thiazol-2-yl)(4-fluorophenyl)methanone(1268700-01-1)

Safety Data

• Hazardous Substances Data: 1268700-01-1(Hazardous Substances Data)

Upstream product

• 1736-67-0 4-fluorophenylacetaldehyde 
• 1004-00-8 4-chloro-2-aminobenzenethiol 
• 2786-51-8 5-chlorobenzo[d]thiazole 
• 352-32-9 p-fluorotoluene 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 403-31-6 4-fluoro-2-hydroxy-acetophenone 
• 95895-33-3 1-(bromoethynyl)-4-fluorobenzene 

Relevant articles and documents

C2-arylacylation of 2H-benzothiazoles with methyl arenes via Selectfluor oxidation

An efficient Selectfluor-oxidative protocol was developed for the direct C2-arylacylation of 2H-benzothiazoles via the radical reaction of 2H-benzothiazoles with methyl arenes. Selectfluor can effectively promote the oxidative cross-coupling without an ex

A multipathway coupled domino strategy: Metal-free oxidative cyclization for one-pot synthesis of 2-acylbenzothiazoles from multiform substrates

A multipathway coupled domino strategy has been developed for the efficient synthesis of 2-acylbenzothiazoles from multiform substrates arylethenes, arylacetylenes, 2-hydroxy-aromatic ketones, and carbinols via four distinct pathways. Through a logical coupled oxidation/heterocyclization domino process, a variety of 2-acylbenzothiazoles were synthesized free of metal in one pot.

Rucl33h2o catalyzed tandem reaction of alkynylbromides with 2-aminothiophenols in water: A convenient synthesis of 2-benzoylbenzothiazoles

RuCl33H2O catalyzed tandem reaction of alkynyl bromides with 2-aminothiophenols mediated by water is shown to represent a convenient synthesis of 2-benzoylbenzothiazoles. In addition, the Ru(iii) catalyst could be readily recovered and efficiently reused together with water up to three times. CSIRO 2011.