Sulochrin

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Identification

Molecular formula
C19H20O6
CAS Number
479-26-5
IUPAC Name
6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid
Molecular Weight
344.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4200g/cm3
Synonyms
(Z)-Mycophenolic Acid
Interesting facts

Interesting Facts about 6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid

This compound, often referred to in literature for its complex structure, represents a fascinating area of study within organic chemistry. Here are some engaging aspects of this compound:

  • Educational Significance: The intricate arrangement of functional groups in its structure makes it an excellent example for students of organic chemistry to analyze reactivity patterns and synthesis pathways.
  • Potential Applications: As a derivative of the isobenzofuran class, this compound could have applications in pharmaceuticals, particularly as a precursor in the synthesis of bioactive molecules.
  • Structure-Activity Relationship (SAR): The presence of multiple hydroxyl and methoxy groups could significantly enhance its biological activity, making it a subject of interest for pharmacology studies.
  • Natural Occurrence: Compounds with similar frameworks are often found in natural products, offering insight into their roles as secondary metabolites in plants.
  • Chemical Synthesis: The synthesis of such a complex molecule typically requires creative and sophisticated methodologies, often involving multi-step reactions and protecting group strategies.

As noted by chemists, "Understanding synthetic pathways opens up new avenues for innovation in medicinal chemistry." This compound exemplifies such opportunity, inviting further exploration into its effects and applications.

In summary, 6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-isobenzofuran-5-yl)-4-methyl-hex-4-enoic acid stands as a testament to the richness of chemical diversity and the endless possibilities it presents in scientific research.

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