104429-45-0

Basic information

• Product Name: 2-Nonen-4-ynal, 3-phenyl-, (2Z)-
• CAS NO: 104429-45-0
• Molecular Formula: C15H16O
• Molecular Weight: 212.291
• Mol File: 104429-45-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Nonen-4-ynal, 3-phenyl-, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nonen-4-ynal, 3-phenyl-, (2Z)-(104429-45-0)
• EPA Substance Registry System: 2-Nonen-4-ynal, 3-phenyl-, (2Z)-(104429-45-0)

Safety Data

• Hazardous Substances Data: 104429-45-0(Hazardous Substances Data)

Upstream product

• 14804-59-2 (Z)-β-bromocinnamaldehyde 
• 693-02-7 hex-1-yne 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 152876-60-3 ethyl (2Z)-3-iodo-3-phenylprop-2-enoate 
• 911047-11-5 ethyl (2Z)-3-phenylnon-2-en-4-ynoate 
• 98-86-2 acetophenone 
• 98-88-4 benzoyl chloride 
• 15724-86-4 E-2-chlorovinyl phenyl ketone 
• 18609-60-4 (Z)-3-hydroxy-1-phenylprop-2-en-1-one 
• 104429-38-1 (E)-1-Chloro-3-phenyl-non-1-en-4-yn-3-ol 

Downstream Products

• 566190-71-4 4-Methyl-N-[(Z)-3-phenyl-non-2-en-4-yn-(E)-ylidene]-benzenesulfonamide 
• 1264272-27-6 C₁₆H₂₀O 
• 1264272-00-5 C₁₈H₂₂O₃ 
• 1257647-25-8 (2E,4Z)-methyl 2-(benzo[d][1,3]dioxole-5-carbonyl)-5-phenylundeca-2,4-dien-6-ynoate 
• 566190-73-6 Benzyl-[(Z)-3-phenyl-non-2-en-4-yn-(E)-ylidene]-amine 
• 566190-70-3 N,N-dimethyl-N'-(3-phenyl-non-2-en-4-ynylidene)-hydrazine 
• 566190-72-5 N-[(Z)-3-Phenyl-non-2-en-4-yn-(E)-ylidene]-methanesulfonamide 

Relevant articles and documents

Palladium-catalyzed alkoxycarbonylation of (Z)-2-en-4-yn carbonates leading to 2,3,5-trienoates

Pd(0)-catalyzed carbonylation of (Z)-2-en-4-yn carbonates in the presence of a balloon pressure of CO in an alcohol donates vinylallenyl esters with an exclusively E-configuration and in high yields. The fact that no such reactivity could be observed with

STEREOSELECTIVE SYNTHESIS AND THERMAL BEHAVIOR OF (Z)-EPOXYHEXENYNES: A SIMPLE AND GENERAL ROUTE TO 2-VINYLFURANS

An efficient approach for the synthesis of 2,3-disubstituted furans (2a-j/3a-j) is described by using the thermally induced rearrangement of epoxyhexenynes (1a-j) which are prepared by streoselective synthesis of the (Z)-pentenynals 10 and subsequent Darz