19066-35-4

Usage

InChI:InChI=1/C20H20N2O/c23-18-20(17-9-5-2-6-10-17)11-19(16-7-3-1-4-8-16)12-21(14-20)15-22(18)13-19/h1-10H,11-15H2

Upstream product

• 50-00-0 formaldehyd 
• 631-61-8 ammonium acetate 
• 102-04-5 1,3-Diphenylpropanone 
• 100-97-0 hexamethylenetetramine 
• 13638-71-6 9-oxo-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonane-3,7-dicarboxylic acid diethyl ester 
• 57164-14-4 1,5-diphenyl-3,7-diazabicyclo<3.3.1>nonan-9-one 

Downstream Products

• 13638-71-6 9-oxo-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonane-3,7-dicarboxylic acid diethyl ester 
• 79168-89-1 3,7-diacetyl-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 102889-39-4 3,7-bis-chloroacetyl-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 38705-08-7 5,7-diphenyl-1,3-diaza-adamantane 
• 98230-08-1 3,7-dinitroso-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 3576-75-8 5,7-diphenyl-1,3-diaza-adamantan-6-ol 
• 57164-14-4 1,5-diphenyl-3,7-diazabicyclo<3.3.1>nonan-9-one 
• 14930-85-9 5,7-diphenyl-1,3-diaza-2-thia-tricyclo[3.3.1.1^3,7]decan-6-one 2-oxide 
• 1604777-44-7 2-chloro-5,7-diphenyl-1,3-diaza-2-phospha-tricyclo[3.3.1.1^3,7]decane-6-one 2-oxide 
• 1604777-55-0 sodium 6-oxo-5,7-diphenyl-1,3-diaza-2-phospha-tricyclo[3.3.1.1^3,7]decan-2-olate 2-oxide 
• 14840-71-2 2,2-dioxo-5,7-diphenyl-2λ⁶-thia-1,3-diaza-adamantan-6-one 
• 14930-85-9 2-oxo-5,7-diphenyl-2λ⁴-thia-1,3-diaza-adamantan-6-one 
• 1053242-62-8 C₂₇H₂₈N₂O₅ 
• 104410-14-2 6-amino-5,7-diphenyl-1,3-diaza-adamantane 

Relevant academic research and scientific papers

Anti-neoplastic activity of 1,3-diaza-2-functionalized-adamantan-6-one compounds against melanoma cells

Four series of 1,3-diaza-2-functionalized-adamantan-6-one derivatives, bearing at the 2 position SO, SO2, POCl and PO2H functional groups, were synthesized via a key quadruple Mannich reaction, followed by transformation of an aminal functionality into th

2,6-DIPHENYL-4,8-DIAZOADAMANTAN-1-ONE AND DERIVATIVES THEREOF, PROCESS OF MANUFACTURE AND USE FOR THE FORMULATION OF SOLUTIONS WITH STERILIZING AND DISINFECTANT EFFECT

A chemical compound having the following structural formula wherein optionally at least one of the phenyl —C6H5 groups bound to the Carbon atoms in position 2 and 6 is independently substituted with a methyl —CH3 or ethyl

Synthesis of novel diazabicycles and their antiprotozoal activities

We describe the synthesis of new diaryl substituted diazabicyclo[3.2.1] octanes from diazepanes which were prepared by the reduction of diazepanones. The formation of the bicyclic system was optimized by microwave irradiation and the structures of the new compounds were established by single crystal structure analysis and NMR spectroscopy. All new compounds were tested for their potencies against Plasmodium falciparum K1 and Trypanosoma b. rhodesiense, the causative organisms of malaria tropica and the East African form of sleeping sickness. CSIRO 2009.

Structural and spatial considerations in the N,N′-diacyl- and bis(alkoxycarbonyl)bispidinone series

(Chemical Equation Presented) Diamidic and dicarbamic bispidinones show trans-cis isomerism, the relative population in solution of the cis form increasing with solvent polarity. The mutual proximity of the two amide functions in 4a has no impact on the b

Conformational Control in the 3,7-Diazabicyclononane System

The twin-chair or boat-chair conformation of 3,7-diazabicyclononanes can be selected by forming N,N'-derivatives in which the N atoms have planar or pyramidal bonding patterns, respectively, e.g., acyl substituents for the former and arylsulphonyl

HETEROADAMANTANES AND THEIR DERIVATIVES. 6. SYNTHESIS AND MASS-SPECTROMETRIC INVESTIGATION OF 5-MONO- AND 5,6-DISUBSTITUTED 6-OXO-1,3-DIAZAADAMANTANES

The corresponding 5-mono and 5,7-disubstituted 6-oxo-1,3-diazaadamantanes were obtained with high yields by the condensation of mono and α,α'-disubstituted acetones with hexamethylenetetramine in the presence of glacial acetic acid, and their structures w