29568-12-5

Basic information

• Product Name: Benzoic acid, 4-ethenyl-, phenyl ester
• CAS NO: 29568-12-5
• Molecular Formula: C15H12O2
• Molecular Weight: 224.259
• Mol File: 29568-12-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-ethenyl-, phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-ethenyl-, phenyl ester(29568-12-5)
• EPA Substance Registry System: Benzoic acid, 4-ethenyl-, phenyl ester(29568-12-5)

Safety Data

• Hazardous Substances Data: 29568-12-5(Hazardous Substances Data)

Upstream product

• 108-95-2 phenol 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 1864-94-4 phenyl formate 
• 1075-49-6 4-ethenylbenzoic acid 

Relevant articles and documents

Palladacycle-catalyzed carbonylation of aryl iodides or bromides with aryl formates

An efficient palladacycle-catalyzed aromatic carbonylation reaction of aryl formates with aryl iodides or bromides has been developed. Commercially available and easily prepared aryl formates were employed as carbonyl sources without the use of external carbon monoxide. The present catalytic system shows broad functional group tolerance and affords aryl benzoate derivatives in good to excellent yields. Copyright

One-pot synthesis of cyclic triamides with a triangular cavity from trans-stilbene and diphenylacetylene monomers

(Chemical Equation Presented) Base-promoted self-condensation reactions of trans-stilbene and diphenylacetylene monomers bearing 4-alkylamino and 4′-methoxycarbonyl groups were investigated. Reactions of N-propyl monomers under pseudohigh-dilution conditions (a THF solution of monomer was added dropwise to a THF solution of LiHMDS) afforded the corresponding cyclic triamides in good yields. X-ray crystallographic analysis showed that these cyclic triamides possessed an almost equilateral triangle structure with a cavity surrounded by tilted benzene rings.