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Trimetamfetamine

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Identification
Molecular formula
C10H21N
CAS number
33716-58-2
IUPAC name
N,N,1,7,7-pentamethylnorbornan-2-amine
State
State

Trimetamfetamine is a liquid at room temperature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
186.00
Boiling point (Kelvin)
459.15
General information
Molecular weight
155.27g/mol
Molar mass
155.2740g/mol
Density
0.8820g/cm3
Appearence

Trimetamfetamine is a colorless liquid with a slight amine odor. It appears clear and free of any solid particles or impurities.

Comment on solubility

Solubility of N,N,1,7,7-pentamethylnorbornan-2-amine

N,N,1,7,7-pentamethylnorbornan-2-amine exhibits unique solubility characteristics largely influenced by its structure. This compound, which features multiple methyl groups, affects its interaction with solvents. Here are some key points about its solubility:

  • Polarity: The presence of amine functional groups increases polarity, which can enhance solubility in polar solvents, particularly water.
  • Hydrophilic vs. Hydrophobic: The bulky pentamethyl structure may hinder solvation, indicating varying solubility in different solvents.
  • Organic Solvents: Often, compounds with similar configurations show greater solubility in organic solvents due to hydrophobic interactions.
  • Temperature Effects: Solubility can be temperature-dependent; increasing temperature usually enhances solubility in many solvents.

In summary, the solubility of N,N,1,7,7-pentamethylnorbornan-2-amine is diverse and context-dependent, showcasing a balance between its polar and nonpolar attributes. Understanding such solubility traits is crucial for applications in various chemical processes.

Interesting facts

Interesting Facts about N,N,1,7,7-Pentamethylnorbornan-2-amine

N,N,1,7,7-Pentamethylnorbornan-2-amine is a fascinating compound that belongs to the class of amines, and it presents a unique structure with intriguing properties.

Key Characteristics

  • Structural Complexity: This compound consists of a norbornane backbone, which is a bicyclic hydrocarbon. The multiple methyl substitutions create steric hindrance, which can significantly alter the reactivity and properties of the amine.
  • Applications in Chemistry: The compound is often studied for its potential applications in organic synthesis, particularly in creating more complex molecules due to its highly reactive amine functional group.
  • Chirality: The presence of chiral centers in its structure means that N,N,1,7,7-pentamethylnorbornan-2-amine can exist in different stereoisomers. This property is essential in medicinal chemistry, as the activity of a drug can differ based on its stereoisomer.

Research and Development

Scientists have shown increasing interest in this compound because:

  • It can serve as a building block for the development of more complex chemical entities.
  • Its derivatives are being studied for their potential pharmacological activities, which may lead to the development of novel pharmaceuticals.

Quote to Remember

As chemists say, "Structure dictates function." The unique structure of N,N,1,7,7-pentamethylnorbornan-2-amine underscores the importance of molecular architecture in influencing reactivity and biological activity.

In summary, N,N,1,7,7-pentamethylnorbornan-2-amine is not just a compound; it is a gateway to exploring the fascinating world of organic chemistry, where structure, functionality, and application converge.

Synonyms
2-Bornanamine, N,N-dimethyl-
22243-41-0
DTXSID50274916
RefChem:256670
DTXCID80226367
N,N,1,7,7-Pentamethylbicyclo[2.2.1]heptan-2-amine
Dimethylbornylamin
2-Bornanamine, N,N-dimethyl-, endo-
CHEMBL268543
XUDICDUSDBRTAJ-UHFFFAOYSA-N
N,N,1,7,7-Pentamethylbicyclo[2.2.1]heptan-2-amine #
Bicyclo[2.2.1]heptan-2-amine, N,N,1,7,7-pentamethyl-, endo-