54644-13-2

Basic information

• Product Name: 5-chloro-2-phenyloxazole-4-carbaldehyde
• Synonyms: 5-chloro-2-phenyloxazole-4-carbaldehyde
• CAS NO: 54644-13-2
• Molecular Weight: 207.616
• Mol File: 54644-13-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-chloro-2-phenyloxazole-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-2-phenyloxazole-4-carbaldehyde(54644-13-2)
• EPA Substance Registry System: 5-chloro-2-phenyloxazole-4-carbaldehyde(54644-13-2)

Safety Data

• Hazardous Substances Data: 54644-13-2(Hazardous Substances Data)

Upstream product

• 96285-99-3 2-phenyl-4-cyano-5-chlorooxazole 
• 40527-16-0 5-methoxy-2-phenyloxazole 
• 68-12-2 N,N-dimethyl-formamide 
• 98-88-4 benzoyl chloride 
• 1205-08-9 methyl hippurate 
• 495-69-2 Hippuric Acid 
• 855404-68-1 5-chloro-2-phenyl-oxazole-4-carbonyl chloride 
• 855405-25-3 5-chloro-2-phenyl-oxazole-4-carboxylic acid 
• 855841-14-4 2-phenyl-5-chloro-1,3-oxazole-4-carboxamide 

Downstream Products

• 60642-60-6 2-phenyl-4-dimethylaminomethyleneoxazole-5-thione 
• 1204-70-2 2-phenyl-1,3-oxazole-4-carbonyl chloride 
• 60642-56-0 2-phenyl-5-thioxo-4,5-dihydro-oxazole-4-carbaldehyde 
• 54644-08-5 3-(5-chloro-2-phenyl-oxazol-4-yl)-acrylic acid ethyl ester 

Relevant articles and documents

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde with vilsmeier reagent

A convenient method for synthesis of 5-chloro-2-aryloxazole-4-carbaldehyde 3 in moderate to good yields had been developed via the Vilsmeier reaction of readily available N-arylglycine 2 at 100 °C, provided a novel route for the construction of nitrogen heterocycles. A series of these compounds were synthesized by this method and optimization of conditions was performed. The Japan Institute of Heterocyclic Chemistry.