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Furfurylamine Dimethylpropane

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Identification
Molecular formula
C9H15NO
CAS number
32115-75-2
IUPAC name
3-(2-furyl)-N,N-dimethyl-propan-1-amine
State
State

The compound is a liquid at room temperature. It is soluble in organic solvents and may exhibit slightly low solubility in water.

Melting point (Celsius)
-21.00
Melting point (Kelvin)
252.15
Boiling point (Celsius)
193.00
Boiling point (Kelvin)
466.15
General information
Molecular weight
167.24g/mol
Molar mass
167.2370g/mol
Density
0.9771g/cm3
Appearence

Furfurylamine Dimethylpropane is a colorless to slightly yellow liquid with a mild odor. It is usually clear and transparent in appearance, making it easily identifiable in laboratories. The liquid may darken upon exposure to air due to oxidation.

Comment on solubility

Solubility of 3-(2-furyl)-N,N-dimethyl-propan-1-amine

The compound 3-(2-furyl)-N,N-dimethyl-propan-1-amine, known for its distinctive structure, exhibits intriguing solubility properties that are vital for its applications.

Factors Influencing Solubility

Several factors contribute to the solubility of this compound:

  • Polarity: The presence of the furyl ring introduces polarity, affecting how it interacts with solvents.
  • Hydrogen Bonding: The amine functional group is capable of forming hydrogen bonds, which can enhance solubility in polar solvents.
  • Chain Length: The propan-1-amine portion adds hydrophobic character, influencing solubility in non-polar environments.

Solvent Compatibility

3-(2-furyl)-N,N-dimethyl-propan-1-amine tends to dissolve well in:

  • Polar solvents: Such as water and alcohols, due to its ability to engage in hydrogen bonding.
  • Non-polar solvents: It may show some solubility, albeit reduced, depending on the solvent's characteristics.

In summary, the solubility of 3-(2-furyl)-N,N-dimethyl-propan-1-amine is a complex interplay of its unique molecular structure and the surrounding environment. As with many organic compounds, understanding these aspects is crucial for practical applications in fields such as pharmaceuticals and materials science.

Interesting facts

3-(2-furyl)-N,N-dimethyl-propan-1-amine: A Unique Chemical Entity

3-(2-furyl)-N,N-dimethyl-propan-1-amine, often referred to for the intriguing properties it embodies, is a compound that intertwines a central amine structure with a furan ring. This fusion of functionalities opens up enticing avenues in fragrance chemistry and pharmaceutical research. Here are some captivating facts about this compound:

  • Furan Component: The presence of the furan ring, a five-membered aromatic compound, gives this amine unique electronic properties, often enhancing its reactivity and stability in organic reactions.
  • Biological Activity: Compounds featuring amine moieties are noteworthy in medicinal chemistry. The subtle modifications in the structure affecting pharmacokinetics could lead to promising biological activity, making it a candidate for further research in drug development.
  • Versatility in Synthesis: The dimethyl functionality introduces significant variance in synthetic pathways, suggesting potential use in designing complex organic molecules through various transformation techniques.
  • Applications in Flavor and Fragrance: The aromatic nature derived from the furan part may contribute to its usefulness in the flavor and fragrance industry, where compounds with specific olfactory characteristics are highly sought after.

As a chemist or student, exploring the structural intricacies and potential applications of 3-(2-furyl)-N,N-dimethyl-propan-1-amine can lead to a deeper understanding of both its synthetic utility and its biological relevance. Remember, compounds like these not only enrich our knowledge but may also hold the keys to groundbreaking innovations in various scientific fields!

Synonyms
N,N-Dimethyl-2-furanpropylamine
2-FURANPROPYLAMINE, N,N-DIMETHYL-
BRN 0116953
25435-32-9
DTXSID40180092
5-18-09-00594 (Beilstein Handbook Reference)
RefChem:261335
DTXCID50102583
1-(alpha-furyl)-3-dimethylaminopropane