183859-96-3

Basic information

• Product Name: 2-Naphthalenecarboxaldehyde, 3,4-dihydro-1-(phenylethynyl)-
• CAS NO: 183859-96-3
• Molecular Formula: C19H14O
• Molecular Weight: 258.32
• Mol File: 183859-96-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Naphthalenecarboxaldehyde, 3,4-dihydro-1-(phenylethynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenecarboxaldehyde, 3,4-dihydro-1-(phenylethynyl)-(183859-96-3)
• EPA Substance Registry System: 2-Naphthalenecarboxaldehyde, 3,4-dihydro-1-(phenylethynyl)-(183859-96-3)

Safety Data

• Hazardous Substances Data: 183859-96-3(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 3262-03-1 1-chloro-2-formyl-3,4-dihydronaphthalene 
• 536-74-3 phenylacetylene 
• 117582-62-4 1-bromo-2-formyl-3,4-dihydronaphthalene 

Downstream Products

• 14385-54-7 phenyl-2 naphto<2,1-b>furanne 
• 1207093-69-3 C₁₉H₁₄O₂ 
• 183860-04-0 4-Nitro-3-phenyl-1-(1-phenylethynyl-3,4-dihydro-naphthalen-2-yl)-butan-1-one 
• 183860-07-3 4-Nitro-1-(1-phenylethynyl-3,4-dihydro-naphthalen-2-yl)-pentan-1-one 
• 183860-08-4 3-Phenyl-5-(1-phenylethynyl-3,4-dihydro-naphthalen-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide 
• 183860-11-9 2-Methyl-5-(1-phenylethynyl-3,4-dihydro-naphthalen-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide 
• 183859-99-6 1-(1-Phenylethynyl-3,4-dihydro-naphthalen-2-yl)-ethanone 
• 183859-97-4 1-(1-Phenylethynyl-3,4-dihydro-naphthalen-2-yl)-ethanol 

Relevant articles and documents

Microwave assisted [RuCl2(p-cymene)2]2 catalyzed regioselective endo-tandem cyclization involving imine and alkyne activation: An approach to benzo[4,5]imidazo[2,1-a]pyridine scaffold

A microwave assisted efficient route to the synthesis of benzimidazole fused heterocycles through metal catalyzed endo-cyclization strategy involving imine and alkyne activation has been developed. In the presence of [RuCl 2(p-cymene)2/su

Synthesis of pyridine-fused ring systems from β-chloroacroleins: A comparison of three different pathways

Three different pathways for the access of pyridine-fused ring systems are described: 1) a Sonogashira coupling of β-chloroacroleins followed by cyclization of the corresponding imines; 2) the same coupling reaction followed by cyclization of the corresponding oximes; and 3) a palladium-catalyzed iminoannulation of internal alkynes.