Fluazifop-P-butyl
- Molecular formula
- C19H20ClNO4
- CAS Number
- 79241-46-6
- IUPAC Name
- 2-morpholinoethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate
- Molecular Weight
- 383.82g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1760g/cm3
Identification
Interesting Facts about 2-Morpholinoethyl 2-(4-Chlorophenoxy)-3-phenyl-prop-2-enoate
2-Morpholinoethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate is a fascinating compound that belongs to a class of organic molecules known for their diverse applications in medicinal chemistry. Here are some notable points about this compound:
- Versatile Applications: This compound can serve as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents.
- Unique Structure: The presence of both a morpholino group and a chlorophenoxy moiety contributes to its unique chemical properties, enhancing its ability to interact with biological targets.
- Biological Activity: Compounds similar to this one have shown potential as inhibitors of certain enzymes, making them candidates for drug development against diseases like cancer or bacterial infections.
- Synthetic Pathways: The synthesis of 2-morpholinoethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate involves several steps, highlighting the intricate processes required to create complex organic molecules.
- Research Interest: Ongoing studies into similar compounds continue to uncover new biological activities, making this field of research highly dynamic and valuable.
As you delve deeper into the chemistry of this compound, consider the broader implications of such research in drug discovery and development. As noted in the scientific community, "The next great medical breakthrough could hinge on the discovery of new compounds that target specific cellular pathways." By studying compounds like 2-morpholinoethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate, chemists are continuously paving the way for innovations in pharmaceuticals.