108120-32-7

Basic information

• Product Name: 1-Naphthalenecarboxaldehyde, 2-[[(2E)-3-phenyl-2-propenyl]oxy]-
• CAS NO: 108120-32-7
• Molecular Formula: C20H16O2
• Molecular Weight: 288.346
• Mol File: 108120-32-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenecarboxaldehyde, 2-[[(2E)-3-phenyl-2-propenyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenecarboxaldehyde, 2-[[(2E)-3-phenyl-2-propenyl]oxy]-(108120-32-7)
• EPA Substance Registry System: 1-Naphthalenecarboxaldehyde, 2-[[(2E)-3-phenyl-2-propenyl]oxy]-(108120-32-7)

Safety Data

• Hazardous Substances Data: 108120-32-7(Hazardous Substances Data)

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 
• 4392-24-9 Cinnamyl bromide 

Downstream Products

• 1191271-34-7 2-benzyl-2,3-dihydro-benzo[f]chromen-1-one 
• 108120-47-4 1,2-diacetyl-1,2,3,3a,4,11c-hexahydronaphtho<1',2',:5,6>pyrano<4,3-c>pyrazole 
• 108120-64-5 2-methyl-2,3,3a,4-tetrahydronaphtho<1',2':5,6>pyrano<4,3-c>pyrazole 
• 108120-42-9 (3R,3aS,11cR)-3-Phenyl-1,2,3,3a,4,11c-hexahydro-5-oxa-1,2-diaza-cyclopenta[c]phenanthrene 
• 108120-69-0 (3R,3aS,11cR)-1,2-Dimethyl-3-phenyl-1,2,3,3a,4,11c-hexahydro-5-oxa-1,2-diaza-cyclopenta[c]phenanthrene 
• 108120-59-8 2-Methyl-2,3-diphenyl-1,2,3,3a,4,11c-hexahydro-5-oxa-1-aza-2-azonia-cyclopenta[c]phenanthrene; chloride 
• 108120-51-0 2,2-Dimethyl-3-phenyl-1,2,3,3a,4,11c-hexahydro-5-oxa-1-aza-2-azonia-cyclopenta[c]phenanthrene; chloride 

Relevant articles and documents

Synthesis of o-Allyloxy(ethynyl)benzene Derivatives by Cu-Catalyzed Suzuki–Miyaura-Type Reaction and Their Transformations into Heterocyclic Compounds

We have found that Suzuki–Miyaura-type reactions of o-allyloxy(bromoethynyl)benzenes with arylboronic acids using a hydrazone/Cu catalyst system proceeded smoothly in iPrOH under mild conditions to afford the corresponding o-allyloxy(arylethynyl)benzene derivatives in good yields without decomposition of the allyloxy group. We have further demonstrated that annulation and enyne metathesis of the o-allyloxy(arylethynyl)benzene derivatives using transition-metal catalysts led to various heterocyclic compounds.