Interesting facts
Exploring 1,7,7-Trimethylnorbornan-2-amine
1,7,7-Trimethylnorbornan-2-amine is a fascinating compound belonging to the class of amines. Its unique structure and properties offer a variety of interesting implications and applications in the field of chemistry:
- Structural Complexity: The compound contains a bicyclic structure with multiple methyl groups attached, contributing to its high degree of steric hindrance. This structure can significantly influence its reactivity and interaction with other molecules.
- Unique Stereochemistry: The arrangement of substituents in 1,7,7-trimethylnorbornan-2-amine can lead to interesting stereochemical properties, which are essential in asymmetric synthesis and drug design. Stereochemistry plays a crucial role in determining the bioactivity of pharmaceutical compounds.
- Application in Organic Synthesis: Compounds like 1,7,7-trimethylnorbornan-2-amine can be utilized as chiral auxiliaries or catalysts in organic synthesis, providing a method for creating complex molecules with high specificity.
- Study of Reaction Mechanisms: The unique electronic and geometric features of the amine functional group within this framework make it an excellent candidate for studying various reaction mechanisms. Understanding these processes is vital for advancements in synthetic organic chemistry.
- Medicinal Chemistry: Amines are foundational in the development of many pharmaceuticals. The study of 1,7,7-trimethylnorbornan-2-amine could lead to insights into new drug formulations, potentially enhancing therapeutic efficacy.
In the words of a renowned chemist, "Understanding the complexities of organic compounds is like unlocking the mysteries of life itself." The multifaceted nature of 1,7,7-trimethylnorbornan-2-amine exemplifies this philosophy, making it a significant topic of inquiry within the scientific community.
Synonyms
(1R,2S,4R)-Born-2-ylamine
EINECS 251-076-9
RefChem:393306
251-076-9
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-amine
Bornylamine
4481-88-3
2-Bornylamine
464-42-6
32511-34-5
MFCD24393344
ENDO-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-AMINE
(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)amine hydrochloride
1,7,7-trimethylnorbornan-2-amine
endo-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-amine
1,7,7-trimethylbicyclo[2.2.1]hept-2-ylamine
Maybridge1_006085
Camphylamin
endo-2-Bornylamine
EINECS 207-351-0
2-Bornanamine, endo-
(1R,4R)-2-Amino-1,7,7-trimethylbicyclo[2.2.1]heptane
Oprea1_727966
SCHEMBL159243
SCHEMBL8651080
DTXSID70954248
SBB072172
STK520676
AKOS005265172
AB90024
SY271823
DB-068643
CS-0311155
NS00089981
ST45027629
EN300-34035
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-amine #
Bicyclo[2.2.1]heptan-2-amine, 1,7,7-trimethyl-, endo-
Solubility Characteristics of 1,7,7-Trimethylnorbornan-2-amine
The solubility of 1,7,7-trimethylnorbornan-2-amine is influenced by its unique structural features and functional groups. As an amine, it possesses a nitrogen atom with a lone pair of electrons, which can participate in hydrogen bonding with water molecules. However, due to its bulky hydrocarbon framework, its solubility is somewhat limited.
Key points regarding its solubility include:
In summary, while 1,7,7-trimethylnorbornan-2-amine can display some degree of water solubility due to its amine functional group, the presence of numerous carbon substituents limits this property. Thus, it is best suited for applications where a higher solubilizing medium, such as organic solvents, is available.