4,6-Dimethyl-2-aminopyridine
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- Molecular formula
- C7H10N2
- CAS Number
- 3430-09-5
- IUPAC Name
- 4,6-dimethylpyridin-2-amine
- Molecular Weight
- 122.17g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0000g/cm3
- Synonyms
- 2-AMINO-4, 6-DIMETHYLPYRIDINE
Identification
Interesting facts
Interesting Facts About 4,6-Dimethylpyridin-2-amine
4,6-Dimethylpyridin-2-amine, also known as 2-amino-4,6-dimethylpyridine, is a fascinating compound that plays an important role in various fields of chemistry and pharmaceuticals. Here are some key points to consider:
- Structural Characteristics: This compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of two methyl groups at the 4 and 6 positions adds to its unique properties and enhances its reactivity.
- Biological Relevance: Pyridine derivatives, including 4,6-dimethylpyridin-2-amine, are frequently investigated for their biological activities. They have shown potential in anti-inflammatory, antimicrobial, and anticancer research.
- Synthesis Approaches: Chemists utilize various methods to synthesize this compound, often starting from available pyridine derivatives. Techniques might include alkylation reactions or functional group modifications.
- Applications: Beyond pharmaceuticals, derivatives of this compound are used in the synthesis of dyes, agrochemicals, and catalysts. Its diverse applications make it a compound of interest in both academic and industrial settings.
- Intriguing Reactions: Due to the electron-rich nature of the amine group, 4,6-dimethylpyridin-2-amine can engage in various organic reactions such as nucleophilic substitutions and coupling reactions, making it valuable in synthetic organic chemistry.
As a chemistry student or researcher, studying compounds like 4,6-dimethylpyridin-2-amine broadens your understanding of organic reactions and their practical applications. Its reactivity and the potential for novel discoveries make it an intriguing topic in chemical research.