33211-90-4

Usage

Uses

Used in Pharmaceutical Industry:
N-octyltricyclo[3.3.1.1~3,7~]decan-1-amine is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, N-octyltricyclo[3.3.1.1~3,7~]decan-1-amine is utilized as an intermediate for the synthesis of agrochemicals. Its cage-like structure contributes to the creation of effective compounds for agricultural applications.
Used in Material Science:
N-octyltricyclo[3.3.1.1~3,7~]decan-1-amine is used as a building block in the development of new materials. Its rigid and bulky molecular structure makes it suitable for creating materials with specific properties for various applications.
Used as a Surface-Active Agent:
In various industrial applications, N-octyltricyclo[3.3.1.1~3,7~]decan-1-amine serves as a surface-active agent. Its ability to interact with surfaces and alter their properties makes it useful in a range of processes, including emulsification, dispersion, and stabilization.

Upstream product

• 768-90-1 1-Adamantyl bromide 
• 1116-76-3 Tri-n-octylamine 
• 768-94-5 1-Adamantanamine 
• 111-86-4 n-Octylamine 
• 1120-48-5 n-dioctylamine 
• 124-12-9 caprylnitrile 
• 16583-95-2 N-((3s,5s,7s)-adamantan-1-yl)octanamide 

Relevant academic research and scientific papers

High fidelity kinetic self-sorting in multi-component systems based on guests with multiple binding epitopes

The molecular recognition platforms of natural systems often possess multiple binding epitopes, each of which has programmed functional consequences. We report the dynamic behavior of a system comprising CB[6], CB[7], and guests cyclohexanediammonium (1) and adamantanealkylammonium (2) that we refer to as a two-faced guest because it contains two distinct binding epitopes. We find that the presence of the two-faced guest-just as is observed for protein targeting in vivo-dictates the kinetic pathway that the system follows toward equilibrium. The influence of two-faced guest structure, cation concentration, cation identity, and individual rate and equilibrium constants on the behavior of the system was explored by a combination of experiment and simulation. Deconstruction of this system led to the discovery of an anomalous host-guest complex (CB[6]·1) whose dissociation rate constant (kout = 8.5 × 10-10 s-1) is ≈100-fold slower than the widely used avidin-biotin affinity pair. This result, in combination with the analysis of previous systems which uncovered extraordinarily tight binding events (Ka ≥ 1012 M-1), highlights the inherent potential of pursuing a systems approach toward supramolecular chemistry.

Ruthenium-catalyzed synthesis of secondary alkylamines: Selective alkylation with aliphatic amines

The chemoselective N-alkylation of tert-alkylamines applying aliphatic amines is described for the first time. In the presence of the Shvo catalyst 1, tert-octylamine 4 and 1-adamantylamine 5 are alkylated using primary, secondary, and even tertiary amine