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3-Isopropylnorbornan-2-amine

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Identification
Molecular formula
C10H19N
CAS number
10380-29-7
IUPAC name
3-isopropylnorbornan-2-amine
State
State

At room temperature, 3-Isopropylnorbornan-2-amine is a liquid. It may solidify upon cooling depending on the environmental temperature.

Melting point (Celsius)
-13.40
Melting point (Kelvin)
259.80
Boiling point (Celsius)
222.30
Boiling point (Kelvin)
495.50
General information
Molecular weight
153.26g/mol
Molar mass
153.2560g/mol
Density
0.8945g/cm3
Appearence

3-Isopropylnorbornan-2-amine appears as a colorless to pale yellow liquid. It typically has a characteristic amine odor. The compound is usually handled in solution or neat depending on the application.

Comment on solubility

Solubility of 3-isopropylnorbornan-2-amine (C10H19N)

The solubility of 3-isopropylnorbornan-2-amine in various solvents plays a crucial role in its applications and chemical behavior. Understanding its solubility can be summarized through the following aspects:

  • Solvent Polarity: This compound is expected to show differing solubility in polar vs. nonpolar solvents. Compounds with amine functional groups typically have better solubility in polar solvents due to hydrogen bonding capabilities.
  • Temperature Influence: Solubility can also change with temperature. Generally, as temperature increases, solubility in water or other polar solvents increases for most organic compounds.
  • pH Effects: The solubility of amines can be affected by the pH of the solution. In acidic conditions, amines can become protonated, which typically increases their solubility in water.

In summary, the solubility of 3-isopropylnorbornan-2-amine can be characterized by its interaction with different solvents, and it tends to be more soluble in polar solvents, especially under acidic conditions. As always, specific experimental conditions should be considered for precise solubility measurements.

Interesting facts

Interesting Facts About 3-Isopropylnorbornan-2-amine

3-Isopropylnorbornan-2-amine is a fascinating organic compound that falls under the category of amines, known for their diverse applications in various fields including pharmaceuticals, agrochemicals, and materials science. Here are some intriguing insights into this compound:

  • Structural Innovation: The unique bicyclic structure of 3-isopropylnorbornan-2-amine results in remarkable properties. The presence of the isopropyl group enhances its steric bulk, contributing to interesting reactivity and stereochemistry.
  • Biological Significance: Compounds like 3-isopropylnorbornan-2-amine often exhibit biological activity, making them valuable in medicinal chemistry. Exploration into its potential as a drug candidate could yield insightful discoveries.
  • Chirality: This compound possesses chiral centers, which means it can exist in multiple enantiomeric forms. Chirality is a critical feature in pharmaceutical development, as different enantiomers can have vastly different biological effects.
  • Synthesis Routes: Synthesizing compounds with complex structures such as 3-isopropylnorbornan-2-amine often involves multiple reaction steps and may require advanced techniques like asymmetric synthesis to obtain the desired enantiomer.
  • Application in Research: 3-Isopropylnorbornan-2-amine serves as a valuable building block in organic synthesis, aiding researchers in developing new chemical entities with enhanced functionalities.

In summary, 3-isopropylnorbornan-2-amine is not only a compound of interest due to its structural complexity but also serves as a cornerstone for ongoing research in areas such as pharmacology and synthetic organic chemistry. As we delve deeper into its properties and applications, it may unveil further scientific opportunities and innovations.

Synonyms
CHEMBL430112
Lopac0_000109
SCHEMBL6777381
BDBM50050094
CCG-204204
3-Isopropyl-bicyclo[2.2.1]hept-2-ylamine
BRD-A79038507-003-02-3
BRD-A79038507-003-03-1