Pirfenidone
- Molecular formula
- C12H11NO2
- CAS Number
- 53179-13-8
- IUPAC Name
- [4-(aminomethyl)-5-hydroxy-6-methyl-3-pyridyl]methyl dihydrogen phosphate
- Molecular Weight
- 185.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5000g/cm3
- Synonyms
- pyridoxamine phosphate
Identification
Interesting Facts about [4-(aminomethyl)-5-hydroxy-6-methyl-3-pyridyl]methyl dihydrogen phosphate
[4-(aminomethyl)-5-hydroxy-6-methyl-3-pyridyl]methyl dihydrogen phosphate is a fascinating compound that belongs to the class of organophosphates. These compounds are crucial in various applications due to their unique properties and functionalities.
Key Features:
- Biological Relevance: This compound is known for its role in biochemical pathways, serving as an important precursor in the synthesis of biologically active molecules.
- Enzyme Inhibition: It can interact with enzymes, influencing metabolic processes and potentially serving as a lead compound for the development of therapeutic agents.
- Versatile Applications: Apart from its biochemical roles, it can be leveraged in agricultural practices, where organophosphate compounds often function as pesticides and herbicides.
The presence of both an amine and a hydroxy group enhances the compound's reactivity, making it an interesting subject of study for synthetic chemists. The structure exhibits a pyridine ring, benefiting from the aromatic stability while providing sites for further chemical modifications.
A Quote to Consider:
As Albert Einstein once said, "Everything should be made as simple as possible, but no simpler." This philosophy often guides chemists as they explore complex compounds like [4-(aminomethyl)-5-hydroxy-6-methyl-3-pyridyl]methyl dihydrogen phosphate, seeking to unravel their mysteries and optimize their applications.
In summary, this compound represents a bridge between organic chemistry and biochemistry, showcasing the interconnectedness of various scientific fields. Further research may reveal even more about its utility and behavior, stimulating curiosity within the scientific community.