15839-23-3

Basic information

• Product Name: Cyclohexanone, 2-[(1-methylethoxy)methylene]-
• CAS NO: 15839-23-3
• Molecular Formula: C10H16O2
• Molecular Weight: 168.236
• Mol File: 15839-23-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-[(1-methylethoxy)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-[(1-methylethoxy)methylene]-(15839-23-3)
• EPA Substance Registry System: Cyclohexanone, 2-[(1-methylethoxy)methylene]-(15839-23-3)

Safety Data

• Hazardous Substances Data: 15839-23-3(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 39695-64-2 2-(hydroxymethylene)cyclohexanone 
• 67-63-0 isopropyl alcohol 
• 75-26-3 isopropyl bromide 
• 823-45-0 2-(hydroxymethylene)cyclohexanone 
• 75-30-9 2-iodo-propane 
• 1193-63-1 Cyclohexanone-2-carbaldehyde 

Downstream Products

• 21336-08-3 3-Oxo-1,5-bis-<2-ethinyl-cyclohexenyl-(1)>-pentadiin-(1,4) 
• 32403-06-8 3-Hydroxy-1,5-bis-<2-ethinyl-cyclohexenyl-(1)>-pentadiin-(1,4) 
• 32166-48-6 1-Ethynyl-2-((E)-hex-1-enyl)-cyclohexene 
• 32166-49-7 1-Ethynyl-2-((Z)-hex-1-enyl)-cyclohexene 
• 21336-06-1 1,2-diethynylcyclohex-1-ene 
• 139459-02-2 Trimethyl-[(Z)-4-(6-phenyl-7-oxa-bicyclo[4.1.0]hept-1-yl)-but-3-en-1-ynyl]-silane 
• 139458-99-4 Trimethyl-[(Z)-4-(2-phenyl-cyclohex-1-enyl)-but-3-en-1-ynyl]-silane 
• 139459-13-5 (2Z,5E)-6-Phenyl-cyclodeca-2,5-diene-1,4-dione 
• 139459-12-4 (E)-3-Phenyl-11-oxa-bicyclo[6.2.1]undeca-1⁽¹⁰⁾,2,8-triene 
• 139459-05-5 1-((Z)-But-1-en-3-ynyl)-6-phenyl-7-oxa-bicyclo[4.1.0]heptane 
• 113388-95-7 3,4,5,6-tetrahydro-[1,1′-biphenyl]-2-carbaldehyde 
• 106180-58-9 (Z)-3-(butano-2-furyl)-4-methyl-2-phenyl-2-pentenenitrile 
• 106180-59-0 (E)-3-(butano-2-furyl)-4-methyl-2-phenyl-2-pentenenitrile 
• 106180-40-9 (Z)-3-<2-(3-Methyl-1-butynyl)-1-cyclohexenyl>-2-phenyloxirane-2-carbonitrile 

Relevant articles and documents

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THERMALLY INITIATED REACTIONS OF (Z)-EPOXYHEXENYNES A FACILE PREPARATION OF 3,4-ANNULATED FURANS

An efficient and general access to 3,4-annulated 2-vinylfurans (type II) is provided by the thermally induced ring transformation of epoxyhexenynes (I).Depending on the substitution pattern the reactions proceed either by heating in solution (5a-h) or under short-time thermolysis conditions (6i, j).The results are consistent with a multistep mechanism involving 1-oxacyclohepta-3,4,6-trienes as central intermediates.

Electrocyclization Rates for Some Donor-Acceptor-Substituted Trienes

Three new trienes, ethyl 3-(2-vinylcyclohexenyl)-trans-propenoate (10), ethyl 3-(2-trans-styrylcyclohexenyl)-trans-propenoate (11), and ethyl 3--trans-propenoate (14), have been prepared and characterized.The kinetic