52917-67-6

Basic information

• Product Name: N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine
• CAS NO: 52917-67-6
• Molecular Formula: C₁₆H₂₁N
• Molecular Weight: 227.3446
• Mol File: 52917-67-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 362.9°C at 760 mmHg
• Flash Point: 182.9°C
• Density: 1.112g/cm³
• Vapor Pressure: 1.87E-05mmHg at 25°C
• Refractive Index: 1.616
• CAS DataBase Reference: N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine(52917-67-6)
• EPA Substance Registry System: N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine(52917-67-6)

Safety Data

• Hazardous Substances Data: 52917-67-6(Hazardous Substances Data)

Usage

General Description

N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine is a complex chemical with a molecular structure comprising a tricyclic ring system fused to a phenyl group and an amine functional group. This chemical is commonly used in research and development of pharmaceuticals and other organic compounds due to its unique structural properties and potential for drug design. It may have potential applications in the development of new medications for various medical conditions. Additionally, N-phenyltricyclo[3.3.1.1~3,7~]decan-2-amine may have industrial uses such as in the production of specialty chemicals or as a building block in organic synthesis processes. However, further research is necessary to fully understand the potential applications and characteristics of this chemical.

Upstream product

• 108-36-1 1,3-dibromobenzene 
• 13074-39-0 N-(2-adamantyl)amine 
• 106-37-6 1.4-dibromobenzene 
• 583-53-9 2,3-dibromobenzene 
• 700-58-3 2-Adamantanone 
• 62-53-3 aniline 
• 700-57-2 1-adamantanol 
• 591-50-4 iodobenzene 

Downstream Products

• 126832-00-6 N-(2-adamantyl)-4-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)aniline 
• 126832-01-7 N-(2-adamantyl)-4-(1-hydroxy-1-methoxycarbonyl-2,2,2-trifluoroethyl)aniline 

Relevant articles and documents

Host-guest assembly of adamantyl tethered squaraine in β-cyclodextrin for monitoring pH in living cells

The formation of a 1:2 inclusion complex between adamantyl tethered squaraine and β-cyclodextrin inhibited the aggregation of SQ in aqueous solution, enhancing the fluorescent emission of the near-infrared dye. The resulting SQ?β-CD complex serves as a sensitive fluorescent probe for imaging intracellular pH in living cells.

Arylation of adamantanamines: IX. Copper(I)-catalyzed arylation of adamantane-containing amines

Copper(I)-catalyzed arylation of 14 adamantane-containing amines with iodobenzene, 1-fluoro-4-iodobenzene, 1-iodo-4-(trifluoromethyl)benzene, and 1-iodo-4-methoxybenzene has been studied under the conditions optimized previously. The yields of the N-aryla

Palladium-catalyzed amination of isomeric dihalobenzenes with 1- and 2-aminoadamantanes

Palladium-catalyzed amination of isomeric bromochloro- and dibromobenzenes with 1- and 2-aminoadamantanes was studied. The best yields of the corresponding monoamination products were obtained in the reactions of 2-aminoadamantane with bromochlorobenzenes