86148-32-5

Basic information

• Product Name: Benzeneethanol, b-methylene-, benzoate
• CAS NO: 86148-32-5
• Molecular Formula: C16H14O2
• Molecular Weight: 238.286
• Mol File: 86148-32-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzeneethanol, b-methylene-, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanol, b-methylene-, benzoate(86148-32-5)
• EPA Substance Registry System: Benzeneethanol, b-methylene-, benzoate(86148-32-5)

Safety Data

• Hazardous Substances Data: 86148-32-5(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 583-04-0 vinyl benzoate 

Downstream Products

• 7283-49-0 2,5-diphenyl-hexa-1,5-diene 
• 31378-03-7 1-phenyl-2-tosylethanone 
• 40240-72-0 (E)-1-(4-methoxyphenyl)-4-phenylbut-2-ene-1,4- dione 
• 1104732-64-0 (E)-1,5-diphenyl-2-tosylpent-4-en-1-one 
• 71899-75-7 2-hydroxy-2-phenylethyl 4-methylphenyl sulfone 
• 23128-65-6 2-bromo-1-phenyl-2-(toluene-4-sulfonyl)ethanone 

Relevant articles and documents

Synthesis of 1,3-diarylpropenes through palladium-catalyzed mizoroki-heck and allyl cross-coupling reactions using hydrazones as ligands

The palladium-catalyzed synthesis of unsymmetrical 1,3-diarylpropenes from allyl esters through a Mizoroki-Heck-type reaction with aryl iodides followed by allyl cross-coupling with a variety of arylboronic acids was developed; the products are obtained in moderate to good yields by using a hydrazone-Pd(OAc) 2 system. The synthesis of unsymmetrical 1,3-diarylpropenes from allyl esters by a Mizoroki-Heck-type reaction followed by allyl cross-coupling with a variety of arylboronic acids was developed; the products were obtained in moderate to good yields by using a hydrazone-Pd(OAc)2 system. Copyright