32729-67-2

Basic information

• Product Name: (5-chloro-1,3-benzothiazol)-2-yl(phenyl)methanone
• Synonyms: (5-chloro-1,3-benzothiazol)-2-yl(phenyl)methanone
• CAS NO: 32729-67-2
• Molecular Weight: 273.743
• Mol File: 32729-67-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: (5-chloro-1,3-benzothiazol)-2-yl(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-chloro-1,3-benzothiazol)-2-yl(phenyl)methanone(32729-67-2)
• EPA Substance Registry System: (5-chloro-1,3-benzothiazol)-2-yl(phenyl)methanone(32729-67-2)

Safety Data

• Hazardous Substances Data: 32729-67-2(Hazardous Substances Data)

Upstream product

• 32771-97-4 (5-chloro-benzothiazol-2-yl)-phenyl-methanol 
• 611-71-2 MANDELIC ACID 
• 1004-00-8 4-chloro-2-aminobenzenethiol 
• 122-78-1 phenylacetaldehyde 
• 7436-90-0 2,2-dibromostyrene 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 100-42-5 styrene 
• 536-74-3 phenylacetylene 
• 582-24-1 1-phenyl-2-hydroxyethanone 
• 98-85-1 1-Phenylethanol 
• 4636-16-2 iodoacetophenone 
• 103-80-0 phenylacetyl chloride 
• 103-82-2 phenylacetic acid 
• 1857-54-1 2-benzyl-5-chlorobenzo[d]thiazole 

Relevant articles and documents

Microwave-assisted controllable synthesis of 2-acylbenzothiazoles and bibenzo[b][1,4]thiazines from aryl methyl ketones and disulfanediyldianilines

A condition-controlled strategy for selectively synthesis of 2-acylbenzothiazoles and bibenzo[b][1,4]thiazines from aryl methyl ketones and disulfanediyldianilines was realized using I2/DMSO or I2/MeCN systems, respectively. The desired products were synthesized in only 15 min with moderate to excellent yields (50%-90%) under microwave-assisted, metal-free conditions. The strategy provides a great advantage for selective synthetic applications in the efficient synthesis of benzothiazoles and bibenzothiazines heterocycle compounds.

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

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;