114078-26-1

Basic information

• Product Name: Furan, 3-[(1E)-2-phenylethenyl]-
• CAS NO: 114078-26-1
• Molecular Formula: C12H10O
• Molecular Weight: 170.211
• Mol File: 114078-26-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Furan, 3-[(1E)-2-phenylethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Furan, 3-[(1E)-2-phenylethenyl]-(114078-26-1)
• EPA Substance Registry System: Furan, 3-[(1E)-2-phenylethenyl]-(114078-26-1)

Safety Data

• Hazardous Substances Data: 114078-26-1(Hazardous Substances Data)

Upstream product

• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 87453-06-3 tributyl(furan-3-yl)stannane 
• 100-42-5 styrene 
• 488-93-7 3-Furoic acid 
• 498-60-2 furan-3-carboxaldehyde 
• 1080-32-6 O,O-diethyl benzylphosphonate 
• 100-44-7 benzyl chloride 
• 100-52-7 benzaldehyde 
• 35731-83-0 (3-furanyl)methyl-triphenylphosphonium bromide 
• 1449-46-3 benzyltriphenylphosphonium bromide 
• 42599-24-6 E-styryl iodide 

Downstream Products

• 1485-07-0 naphthalen-2-ethanol 
• 91-57-6 2-Methylnaphthalene 
• 70080-13-6 2-naphthylacetaldehyde 
• 66-99-9 β-naphthaldehyde 
• 114078-50-1 (E,E)-methyl 3-methoxy-2-(3-styryl-2-furyl)propenoate 

Relevant articles and documents

A new insight into the push-pull effect of substituents via the stilbene-like model compounds

In this paper, authors report on 1-pyridyl-2-arylethenes, 1-furyl-2-arylethylenes, 1,2-diphenylpropylenes and substituted cinnamyl anilines as stilbene-like model compounds to investigate the factors dominating the push-pull effect of substituents via usi

Construction of polyaromatics via photocyclization of 2-(fur-3-yl) ethenylarenes, using a 3-furyl group as an isopropenyl equivalent synthon

The construction of different types of substituted arenes was demonstrated through the photocyclization of 2-(fur-3-yl)ethenylarenes using a 3-furyl group as an isopropenyl equivalent synthon in the photocyclization reaction. The furan portion of the photocyclization intermediate could be fragmented via a base-induced elimination reaction to yield a series of substituted polyaromatics, including naphthalene, benzofuran, benzothiophene, phenanthrene, phenalene, acenaphthene, and triphenylene. Using different reagents, this method made it possible to introduce methyl or 2-hydroxyethyl groups as substituents at specific positions in these arenes.

Development of new Wittig reagent, silylfuranmethylid, and its reactivity

New Wittig reagents, furanmethylids b-e were successfully developed. Their preparation, reactivity, and application toward the natural products synthesis are described in detail.