Squalamine
- Molecular formula
- C30H49NO
- CAS Number
- 142920-48-5
- IUPAC Name
- N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine
- Molecular Weight
- 384.65g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0123g/cm3
- Synonyms
- SCHEMBL3951138
Identification
N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine
N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine is a fascinating organic compound with notable applications in various fields, including biochemistry and materials science. As a member of the amine family, this compound offers several intriguing characteristics and uses:
- Functionality: The presence of multiple methyl groups contributes to the compound's hydrophobicity, influencing its interactions and solubility properties. This hydrophobic nature can enhance its utility in formulating specialized materials.
- Biological Relevance: The structure of this compound suggests potential applications in pharmaceutical chemistry. The triene system may allow the compound to exhibit biological activity akin to natural compounds found in living organisms.
- Synthetic Versatility: The synthesis of N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine illustrates the creativity involved in organic synthesis, showcasing how chemists can manipulate fundamental building blocks to create complex structures.
- Polymer Precursor: Due to its functional groups, this compound may serve as a precursor for creating polymers with tailored properties, which can be utilized in coatings, adhesives, and other industrial applications.
In the words of a renowned chemist, “The beauty of chemistry lies in its ability to transform simple molecules into complex systems.” This compound is a perfect example of how molecular transformations can lead to materials with unique characteristics.
Overall, N,3,7,11-tetramethyldodeca-2,6,10-trien-1-amine is not just a compound; it is a gateway to a myriad of scientific explorations and innovations, embodying the dynamic nature of chemical research.