51496-94-7

Basic information

• Product Name: Benzene, 1-(phenylmethoxy)-2-(2-propenyl)-
• CAS NO: 51496-94-7
• Molecular Formula: C16H16O
• Molecular Weight: 224.302
• Mol File: 51496-94-7.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(phenylmethoxy)-2-(2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(phenylmethoxy)-2-(2-propenyl)-(51496-94-7)
• EPA Substance Registry System: Benzene, 1-(phenylmethoxy)-2-(2-propenyl)-(51496-94-7)

Safety Data

• Hazardous Substances Data: 51496-94-7(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 1745-81-9 o-Allylphenol 
• 100-39-0 benzyl bromide 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 179253-16-8 2-(2-(benzyloxy)phenyl)acetaldehyde 

Downstream Products

• 19997-53-6 (2,3-dihydro-2-benzofuranyl)-methyl bromide 
• 927822-13-7 2-(2-(benzyloxy)phenyl)-3-methyloxirane 
• 927822-12-6 (E)-1-(benzyloxy)-2-(prop-1-enyl)benzene 
• 1442460-54-9 3-(2-(benzyloxy)phenyl)-2-(1,3-dioxoisoindolin-2-yl)propyl acetate 
• 1745-81-9 o-Allylphenol 
• 1094215-68-5 1-(benzyloxy)-5-bromonaphthalene 
• 128923-95-5 1-(benzyloxy)-5-chloronaphthalene 

Relevant articles and documents

Ether bond breakage method for phenylalkyl ethers

The invention discloses an ether bond breakage method for phenylalkyl ethers. The method comprises the step: subjecting the phenylalkyl ethers to an ether bond breakage reaction at the temperature of -20 DEG C to reflux temperature in an organic solvent in the presence of aluminum triiodide and carbodiimide, so as to produce phenols and derivatives thereof. The method is moderate in conditions, simple and convenient in operation, high in yield and wide in applicable phenylalkyl ether range.

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,

The attempted stereoselective synthesis of chiral 2,2′-biindoline

The attempted first stereoselective synthesis of 2,2′-biindoline using a metathesis-Sharpless asymmetric dihydroxylation strategy results in the synthesis of the heterocycle in poor to modest stereoselectivity. Attempts to improve the ee by varying the he