Sodium 2-(4-allyloxy-3-chlorophenyl)acetate
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- Molecular formula
- C11H10ClNaO3
- CAS Number
- 73384-59-5
- IUPAC Name
- sodium;2-(4-allyloxy-3-chloro-phenyl)acetate
- Molecular Weight
- 246.66g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2400g/cm3
Identification
Interesting facts
Interesting Facts about Sodium 2-(4-Allyloxy-3-chloro-phenyl)acetate
Sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is a fascinating compound that showcases the intersection of organic chemistry and medicinal applications. Here are some noteworthy points:
- Structural Complexity: This compound features an intricate structure that includes both an allyloxy group and a chloro-substituted aromatic ring, making it a subject of interest in synthetic organic chemistry.
- Potential Therapeutic Uses: Research has indicated that compounds of this class may possess biological activities, leading to exploration within pharmaceutical chemistry for potential applications in drug development.
- Versatility: The allyloxy moiety can engage in various chemical reactions, making this compound a useful intermediate in organic synthesis and possibly leading to the development of new derivatives.
- Chemical Reactions: The presence of a chloro substituent on the phenyl ring suggests that this compound could participate in nucleophilic substitution reactions, which is a fundamental concept in organic synthesis.
- Environmental Impact: As with many chemical compounds, understanding the environmental behavior of sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is crucial for assessing its safety and ecological effects when used in industrial or laboratory settings.
In sum, sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is more than just a chemical entity; it serves as a gateway to discussions on medicinal chemistry, organic synthesis, and environmental considerations. As one would quote, "Every compound tells a story, and this one hints at the potential for a remarkable narrative in the realm of pharmaceuticals."