27944-89-4

Basic information

• Product Name: 3-(cyclohex-1-en-1-yl)propiolic acid
• Synonyms: 3-(cyclohex-1-en-1-yl)propiolic acid
• CAS NO: 27944-89-4
• Molecular Weight: 150.177
• Mol File: 27944-89-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(cyclohex-1-en-1-yl)propiolic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(cyclohex-1-en-1-yl)propiolic acid(27944-89-4)
• EPA Substance Registry System: 3-(cyclohex-1-en-1-yl)propiolic acid(27944-89-4)

Safety Data

• Hazardous Substances Data: 27944-89-4(Hazardous Substances Data)

Upstream product

• 931-49-7 1-ethenylcyclohexene 
• 124-38-9 carbon dioxide 
• 6482-39-9 sodium methyl carbonate 
• 1192-88-7 1-cyclohexene-1-carboxaldehyde 
• 27944-90-7 methyl 3-(1-cyclohexen-1-yl)-2-propynoate 
• 15719-64-9 methylammonium carbonate 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 16616-44-7 3-(cyclohex-1-en-1-yl)-1-phenylprop-2-yn-1-one 
• 65311-23-1 2-cyclohex-1-en-1-yl-2-oxoethyl acetate 
• 56453-88-4 (E)-3-(1-cyclohexen-1-yl)-2-propenoic acid 
• 85437-89-4 (Z)-3-(cyclohex-1-en-1-yl)acrylic Acid 
• 94002-02-5 3--3-phenoxy-acrylsaeure 
• 93015-56-6 3--3-phenoxy-acrylsaeure-methylester 
• 35354-47-3 3-(1-Cyclohexenyl)-2-propinanilid 
• 35354-46-2 N,N-Diisopropyl-3-(1-cyclohexenyl)-2-propinamid 
• 35354-45-1 N,N-Diethyl-3-(1-cyclohexenyl)-2-propinamid 
• 35354-41-7 3-(1-Cyclohexenyl)-2-propinoyl-chlorid 
• 27944-90-7 methyl 3-(1-cyclohexen-1-yl)-2-propynoate 

Relevant articles and documents

Sodium Methyl Carbonate as an Effective C1 Synthon. Synthesis of Carboxylic Acids, Benzophenones, and Unsymmetrical Ketones

Reported is the synthesis of carboxylic acids, symmetrical ketones, and unsymmetrical ketones with selectivity achieved by exploiting the differential reactivity of sodium methyl carbonate with Grignard and organolithium reagents.

Palladium-Catalyzed Synthesis of Conjugated Allenynes via Decarboxylative Coupling

A new strategy to access conjugated allenynes via a decarboxylative coupling of propargyl esters of propiolates has been developed. In this process, allenyl-palladium intermediates are coupled with acetylides that are generated in situ to form the conjuga