Myosmine
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- Molecular formula
- C7H13N
- CAS Number
- 532-12-7
- IUPAC Name
- N,6-dimethylhept-5-en-2-amine
- Molecular Weight
- 125.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.8896g/cm3
- Synonyms
- Isometheptene
Identification
Interesting facts
Interesting Facts about N,6-dimethylhept-5-en-2-amine
N,6-dimethylhept-5-en-2-amine is a fascinating compound that belongs to the class of organic amines, which are notable for their diverse applications in chemistry and biology. Here are some intriguing aspects of this compound:
- Structural Features: The name indicates the presence of a heptene backbone, characterized by a seven-carbon chain with a double bond, specifically located between the fifth and sixth carbons. This unique structure contributes to its reactivity and physical properties.
- Functional Groups: Being an amine, it contains a nitrogen atom bonded to carbon atoms, which makes it a potential base. Amines are pivotal in organic synthesis and can act as nucleophiles in various chemical reactions.
- Synthetic Utility: Compounds like N,6-dimethylhept-5-en-2-amine may be used as intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Their structural uniqueness allows for the development of new chemical entities.
- Chemical Diversity: The presence of both an alkene and an amine in its structure positions N,6-dimethylhept-5-en-2-amine as a versatile reactant, facilitating various addition reactions essential for constructing complex molecular architectures.
- Biological Implications: Due to the biological relevance of amines, compounds like this one might interact with various biological systems, making them subjects of study in drug design and development.
As a chemistry student or researcher, exploring the potential applications and reactions involving N,6-dimethylhept-5-en-2-amine can lead to a deeper understanding of organic synthesis and the significance of functional groups in the development of innovative chemical products.