67191-36-0

Basic information

• Product Name: Benzene, 1-ethenyl-2-(phenylmethoxy)-
• CAS NO: 67191-36-0
• Molecular Formula: C15H14O
• Molecular Weight: 210.276
• Mol File: 67191-36-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1-ethenyl-2-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-ethenyl-2-(phenylmethoxy)-(67191-36-0)
• EPA Substance Registry System: Benzene, 1-ethenyl-2-(phenylmethoxy)-(67191-36-0)

Safety Data

• Hazardous Substances Data: 67191-36-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 90-02-8 salicylaldehyde 
• 142523-69-1 1-benzyloxy-2-iodobenzene 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 5896-17-3 2-(phenylmethoxy)benzaldehyde 
• 19493-09-5 Methylenetriphenylphosphorane 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 1603829-66-8 C₁₉H₂₁ClOS₂ 
• 645405-50-1 2-(2-(benzyloxy)phenyl)propanal 
• 7462-25-1 2-(benzyloxy)-1-ethylbenzene 
• 1315340-92-1 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole 

Relevant articles and documents

SULFAMATE DERIVATIVE COMPOUNDS FOR USE IN TREATING OR ALLEVIATING PAIN

The present invention relates to sulfamate derivative compounds and a composition for treating and/or alleviating pain containing the sulfamate derivative compounds or a pharmaceutically acceptable salt thereof as an active ingredient. More specifically,

Chemo-, Regio-, and stereoselective trifluoromethylation of styrenes via visible light-driven single-electron transfer (SET) and triplet-triplet energy transfer (TTET) processes

A process for tunable and chemo-, regio-, and stereoselective photocatalytic trifluoromethylation of styrenes was developed. Thermodynamically stable E-trifluoromethylated alkenes were prepared using Tognis reagent in the presence of Ru(bpy)3Cl2·6H2O under visible light irradiation, whereas less thermodynamically stable Z-trifluoromethylated alkenes were obtained by employing Umemotos reagent and photocatalyst Ir(ppy)3.

Efficient heterogeneous vinylation of aryl halides using potassium vinyltrifluoroborate

An efficient heterogeneously palladium catalysed procedure for the vinylation of aryl iodides and bromides is reported. Using common reaction conditions (Pd/C 2 mol %, AcONa·3H2O, NMP or NMP/H2O), good to complete conversions (40-100%) with high selectivities (79-100%) towards the expected vinylaromatic were achieved.