4-(5-fluoro-2-hydroxyphenyl)thiobut-1-enylphosphonic acid
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- Molecular formula
- C10H12FO4P
- CAS Number
- 102212-25-3
- IUPAC Name
- 4-(5-fluoro-2-hydroxy-phenyl)sulfanylbut-1-enylphosphonic acid
- Molecular Weight
- 256.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4510g/cm3
- Appearance
- may vary slightly based on purity and form but generally maintains a uniform powder consistency suitable for research or industrial use.
- Synonyms
- PD036614
Identification
Interesting facts
Exploring 4-(5-fluoro-2-hydroxy-phenyl)sulfanylbut-1-enylphosphonic acid
4-(5-fluoro-2-hydroxy-phenyl)sulfanylbut-1-enylphosphonic acid is a fascinating compound that showcases the intricate interplay between organic chemistry and medicinal applications. Here are some intriguing facts about this compound:
- Functional Diversity: This compound features diverse functional groups, including a phosphonic acid moiety, which is known for its potential in biological systems and its use in drug development.
- Fluorine's Role: The presence of a fluorine atom not only enhances the compound's lipophilicity but may also influence its biological activity, making it a subject of interest in pharmaceutical research.
- Phenolic Hydroxy Group: The 2-hydroxy group on the aromatic ring contributes to the compound's potential as a ligand in complexation with metal ions, which is relevant in catalysis and various synthetic applications.
- Applications in Medicine: Compounds with phosphonic acid groups are often explored for their antibacterial, antiviral, and anticancer properties. This positions 4-(5-fluoro-2-hydroxy-phenyl)sulfanylbut-1-enylphosphonic acid as a candidate for further investigation in drug discovery.
- Molecular Geometry: The geometric arrangement of the compound's atoms can lead to different isomers, each potentially exhibiting unique properties, which is a key consideration in the design of pharmaceuticals.
- Mechanistic Studies: Understanding the interactions and mechanisms of action of this compound can lend insights into the design of more effective therapies, particularly regarding phosphonate derivatives.
In summary, 4-(5-fluoro-2-hydroxy-phenyl)sulfanylbut-1-enylphosphonic acid is more than just a molecular entity; it represents a bridge between chemical synthesis and the quest for new therapeutic solutions. As research into its properties and applications advances, we may uncover even more exciting potential for this compound in various fields of science.