105808-39-7

Basic information

• Product Name: 3-Cyclopenten-1-one, 2-[[5-(4-morpholinyl)-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl]-2,3,4 ,5-tetraphenyl-, cis-
• CAS NO: 105808-39-7
• Molecular Formula: C42H35N5O4
• Molecular Weight: 673.771
• Mol File: 105808-39-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Cyclopenten-1-one, 2-[[5-(4-morpholinyl)-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl]-2,3,4 ,5-tetraphenyl-, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclopenten-1-one, 2-[[5-(4-morpholinyl)-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl]-2,3,4 ,5-tetraphenyl-, cis-(105808-39-7)
• EPA Substance Registry System: 3-Cyclopenten-1-one, 2-[[5-(4-morpholinyl)-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl]-2,3,4 ,5-tetraphenyl-, cis-(105808-39-7)

Safety Data

• Hazardous Substances Data: 105808-39-7(Hazardous Substances Data)

Upstream product

• 479-33-4 2,3,4,5-tetraphenylcyclopenta-2,4-dienone 
• 107090-34-6 5-morpholinomethylene-1,2,3,4-tetraphenyl-bicyclo(2.2.1)hept-2-en-7-one 
• 107090-32-4 exo-7-oxo-1,4,5,6-tetraphenylbicyclo(2.2.1)hept-5-en-2-carboxaldehyde 
• 74073-15-7 4,5-Dihydro-4-methylene-5-morpholino-1-(4-nitrophenyl)-ν-triazole 
• 105808-38-6 C₄₂H₃₅N₅O₄ 
• 1516-60-5 4-nitrophenyl azide 
• 110-91-8 morpholine 
• 105808-39-7 (2S,5R)-2-[5-Morpholin-4-yl-1-(4-nitro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-2,3,4,5-tetraphenyl-cyclopent-3-enone 

Downstream Products

• 114026-62-9 (4R^*,5R^*)-5-<5-morpholino-1-(4-nitrophenyl)-v-triazol-4-yl>methyl-2,3,4,5-tetraphenyl-2-cyclopent-1-one 
• 114026-63-0 5-hydroperoxy-2-<5-morpholino-1-(4-nitrophenyl)-v-triazol-4-yl>methyl-2,3,4,5-tetraphenyl-3-cyclopenten-1-one 
• 105808-39-7 (2S^*,5S^*)-2-<5-morpholino-1-(4-nitrophenyl)-v-triazol-4-yl>methyl-2,3,4,5-tetraphenyl-3-cyclopenten-1-one 

Relevant articles and documents

v-TRIAZOLINES. PART XXVII. ISOMERIZATION REACTIONS OF SUBSTITUTED METHYL-CYCLOPENTEN-3- AND -2-ONES.

Substituted 3-cyclopenten-1-ones 2a,b, derived from the rearrangement of 1, were isomerized under thermal conditions to afford the corresponding 2-cyclopent-1-ones 4, 5b, respectively.When the isomerization was performed with basic catalysis, 2a afforded

v-TRIAZOLINES. Part XXIII. CYCLOADDITION REACTIONS OF 4-NITROPHENYLAZIDE TO ENAMINES OF 1,4,5,6-TETRAPHENYL-7-OXO-BICYCLOHEPT-5-EN-2-CARBOXALDEHYDE

Reaction of 4-nitrophenylazide with the enamines 5, 6 of 7-oxo-1,4,5,6-tetraphenylbicyclohept-5-en-carboxaldehyde 3, 4 which may be isolated or prepared in situ from the aldehyde and the appropiate amine, resulted in the formation of a mixture of t