111904-71-3

Basic information

• Product Name: ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4-oxocyclohexane-1(e)-carboxylate
• Synonyms: ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4-oxocyclohexane-1(e)-carboxylate
• CAS NO: 111904-71-3
• Molecular Weight: 347.414
• Mol File: 111904-71-3.mol

Chemical Properties

• CAS DataBase Reference: ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4-oxocyclohexane-1(e)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4-oxocyclohexane-1(e)-carboxylate(111904-71-3)
• EPA Substance Registry System: ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4-oxocyclohexane-1(e)-carboxylate(111904-71-3)

Safety Data

• Hazardous Substances Data: 111904-71-3(Hazardous Substances Data)

Upstream product

• 35225-79-7 dibenzylideneacetone 
• 105-56-6 ethyl 2-cyanoacetate 
• 538-58-9 1,5-diphenyl-1,4-pentadiene-3-one 

Downstream Products

• 111904-79-1 ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4(e)-acetoxycyclohexane-1-carboxylate 
• 111904-75-7 trans-2(e),6(a)-diphenyl-4,4-(ethylenedioxy)cyclohexane-1(e)-carbonitrile 
• 111904-77-9 4-cyano-trans-5,8-diphenyl-2-oxabicyclo<2.2.2>octan-3-one 
• 111904-78-0 methyl 1-cyano-2(e),6(a)-diphenyl-4(e)-hydroxycyclohexane-1(e)-carboxylate 
• 111904-72-4 ethyl 1-cyano-cis-2(e),6(e)-diphenyl-4-oxocyclohexane-1(e)-carboxylate 
• 111904-73-5 ethyl 1-cyano-trans-2(e),6(a)-diphenyl-4,4-(ethylenedioxy)cyclohexane-1(e)-carboxylate 

Relevant articles and documents

Bio-Catalytic Bis-Michael Reaction for Generating Cyclohexanones with a Quaternary Carbon Center Using Glucoamylase

Abstract: Bio-catalytic bis-Michael reaction for the construction of quaternary carbon centers is reported. Glucoamylase from Aspergillus niger (AnGA) was used as a sustainable and eco-friendly catalyst. Various highly substituted trans-cyclohexanones wit

Asymmetric organocatalytic double-conjugate addition of malononitrile to dienones: Efficient synthesis of optically active cyclohexanones

9-Amino-9-deoxyepiquinine efficiently catalyzed the double-conjugate addition of malononitrile to dienones. A number of 1,1,2,6-tetrasubstituted cyclohexanones were prepared in good yields, diastereoselectivities, and excellent enantioselectivities.