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Camphoramine

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Identification
Molecular formula
C11H19NO
CAS number
504-02-9
IUPAC name
N-(1,7,7-trimethylnorbornan-2-yl)formamide
State
State

At room temperature, Camphoramine is typically found in a solid state.

Melting point (Celsius)
147.00
Melting point (Kelvin)
420.00
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.00
General information
Molecular weight
181.27g/mol
Molar mass
181.2720g/mol
Density
1.0220g/cm3
Appearence

Camphoramine typically appears as a white crystalline solid.

Comment on solubility

Solubility of N-(1,7,7-trimethylnorbornan-2-yl)formamide

N-(1,7,7-trimethylnorbornan-2-yl)formamide exhibits a unique solubility profile influenced by its molecular structure and functional groups. Understanding its solubility characteristics is crucial for various applications.

  • Polar Nature: The presence of the formamide functional group suggests that this compound has polar characteristics, which can enhance its solubility in polar solvents such as water and alcohols.
  • Hydrophobic Characteristics: Conversely, the bulky norbornane structure introduces hydrophobic traits, which may limit its solubility in highly polar solvents.
  • Solvent Interaction: The overall solubility is expected to vary significantly depending on the solvent used. It may dissolve well in solvents like:
    • Alcohols
    • Aromatic hydrocarbons
    • Chloroform

As with many chemical compounds, temperature and concentration also play pivotal roles in determining solubility. Increased temperature often leads to higher solubility, while concentrated solutions may precipitate undissolved material.

In conclusion, the solubility behavior of N-(1,7,7-trimethylnorbornan-2-yl)formamide showcases a delicate balance between its polar and non-polar characteristics, making it an intriguing subject for further investigation in chemical solubility dynamics.

Interesting facts

Exploring N-(1,7,7-trimethylnorbornan-2-yl)formamide

N-(1,7,7-trimethylnorbornan-2-yl)formamide is a fascinating compound that belongs to the category of amides, characterized by the presence of a carbonyl group directly connected to a nitrogen atom. This unique structure gives it several intriguing properties and applications in the field of chemistry.

Significance in Organic Chemistry

One of the notable aspects of N-(1,7,7-trimethylnorbornan-2-yl)formamide is its role as an intermediary in synthetic organic chemistry. Its structural features allow for:

  • Versatile Reactivity: The amide functional group is known for its stability and can undergo various transformations, making it valuable in the synthesis of more complex molecules.
  • Potential as a Ligand: Given its unique molecular architecture, this compound may be explored as a ligand in metal coordination chemistry, leading to novel complexes with interesting properties.

Biological Implications

While not extensively studied, compounds with similar structural frameworks often exhibit biological activities. Here are a couple of areas where this compound might hold potential:

  • Pharmacology: There could be unexplored pharmacological implications, where derivatives of similar amides show promise in drug development.
  • Biochemical Pathways: Its presence in certain biochemical pathways might lead to the discovery of new mechanisms or interactions in physiological systems.

Future Directions

Scientists are always on the lookout for compounds that can yield new insights into chemical reactivity and biological activity. N-(1,7,7-trimethylnorbornan-2-yl)formamide could:

  • Inspire Synthetic Pathways: Its structure may give rise to innovative synthetic methodologies that could simplify the preparation of complex, functionalized molecules.
  • Encourage Further Research: Exploring its properties might open doors to new applications in materials science or biochemistry.

In summary, while N-(1,7,7-trimethylnorbornan-2-yl)formamide might seem niche, its structural uniqueness and potential applications make it a topic of interest for chemists aiming to expand the frontiers of organic synthesis and medicinal chemistry. These explorations not only enhance our understanding of amide compounds but can also lead to significant advancements in science.

Synonyms
(+-)-endo-N-(2-Bornyl)formamide
FORMAMIDE, N-(2-BORNYL)-, endo-(+-)-
24629-79-6
RefChem:345662
Formylbornylamin
SCHEMBL6322514
DTXSID60947548
AKOS014320373
1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-YLFORMAMIDE
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)methanimidic acid