1268700-07-7

Basic information

• Product Name: (4-methoxyphenyl)(6-methylbenzo[d]thiazol-2-yl)methanone
• Synonyms: (4-methoxyphenyl)(6-methylbenzo[d]thiazol-2-yl)methanone
• CAS NO: 1268700-07-7
• Molecular Weight: 283.351
• Mol File: 1268700-07-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (4-methoxyphenyl)(6-methylbenzo[d]thiazol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methoxyphenyl)(6-methylbenzo[d]thiazol-2-yl)methanone(1268700-07-7)
• EPA Substance Registry System: (4-methoxyphenyl)(6-methylbenzo[d]thiazol-2-yl)methanone(1268700-07-7)

Safety Data

• Hazardous Substances Data: 1268700-07-7(Hazardous Substances Data)

Upstream product

• 5703-26-4 4-Methoxyphenylacetaldehyde 
• 23451-96-9 2-amino-5-methylthiophenol 
• 60512-57-4 1-(2,2-dibromovinyl)-4-methoxybenzene 
• 33675-41-1 1-bromo-2-(4-methoxyphenyl)acetylene 
• 106-49-0 p-toluidine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 31183-91-2 2-[(2-amino-5-methylphenyl)dithio]-4-methylphenylamine 

Relevant articles and documents

New synthesis of 2-aroylbenzothiazolesviametal-free domino transformations of anilines, acetophenones, and elemental sulfur

A new synthesis of 2-aroylbenzothiazolesviaiodine-promoted domino transformations of anilines, acetophenones, and elemental sulfur was demonstrated. The highlights of this tandem synthesis are (1) easily available anilines and acetophenones as feedstock;

Synthesis of 2-Acylbenzothiazoles via the Cu(OTf)2-Catalyzed tandem reaction of β,β-Dihalidestyrenes with 2,2′- Disulfanediyldianilines

A new method has been developed for the one-pot construction of 2-acylbenzothiazoles via the Cu(OTf)2-catalyzed tandem reaction of β,β-dihalidestyrenes with 2,2′-disulfane-diyldianilines. A variety of different dihalidestyrenes and diphenyldisulfanes were efficiently converted into the corresponding 2-acylbenzothiszole derivatives in the presence of Cu(OTf)2. Most importantly, this protocol allowed for the long chain 1,1-dibromohept-1-ene to be converted into the corresponding 2-hexylbenzo[d]thiazole in moderate yield. Georg Thieme Verlag Stuttgart, New York.

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.