79146-99-9

Basic information

• Product Name: 4-chloro-N-(1,3-thiazol-2-yl)benzamide
• Synonyms: benzamide, 4-chloro-N-2-thiazolyl-; N1-(1,3-thiazol-2-yl)-4-chlorobenzamide
• CAS NO: 79146-99-9
• Molecular Formula: C₁₀H₇ClN₂OS
• Molecular Weight: 238.6934
• Mol File: 79146-99-9.mol
• Article Data: 5

Chemical Properties

• Density: 1.464g/cm³
• Refractive Index: 1.688
• CAS DataBase Reference: 4-chloro-N-(1,3-thiazol-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-(1,3-thiazol-2-yl)benzamide(79146-99-9)
• EPA Substance Registry System: 4-chloro-N-(1,3-thiazol-2-yl)benzamide(79146-99-9)

Safety Data

• Hazardous Substances Data: 79146-99-9(Hazardous Substances Data)

Upstream product

• 96-50-4 2-thiazolylamine 
• 1871-38-1 phenyl 4-chlorobenzoate 
• 122-01-0 4-chloro-benzoyl chloride 
• 104-88-1 4-chlorobenzaldehyde 
• 59775-49-4 2-<(p-chlorobenzylidene)amino>thiazole 
• 637-87-6 1-Chloro-4-iodobenzene 
• 124-38-9 carbon dioxide 

Downstream Products

• 13159-90-5 (4-chloro-benzyl)-thiazol-2-yl-amine 

Relevant articles and documents

Aminothiazoles and aminothiadiazoles as nucleophiles in aminocarbonylation of iodobenzene derivatives

Various 2-, 3- and 4-substituted iodobenzenes were aminocarbonylated using aminothiazole and aminothiadiazole derivatives in palladium-catalysed reaction. The reaction is chemospecific toward the corresponding carboxamides. Consequently, the application o

Access to Amide from Aldimine via Aerobic Oxidative Carbene Catalysis and LiCl as Cooperative Lewis Acid

Herein, an efficient route to amides from aldimines via aza-Breslow intermediates through aerobic oxidative carbene catalysis with LiCl as a cooperative Lewis acid is described. Many of the obtained N-heteroarylamides feature biological activity. Ambient

Mesoionic purinone analogues as inhibitors of cyclic-AMP phosphodiesterase: A comparison of several ring systems

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