3-(4-Butoxy-3-methoxyphenyl)-2-methylprop-2-enhydroxamic acid

ADVERTISEMENT

Identification

Molecular formula
C15H21NO4
CAS Number
50754-69-5
IUPAC Name
3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid
Molecular Weight
295.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1560g/cm3
Interesting facts

Interesting Facts about 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid

The compound 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid, often referred to in its shorter name, has garnered interest in the fields of medicinal chemistry and drug development. Here are some key points that highlight its significance:

  • Functional Versatility: This compound features hydroxamic acid functionality, which is known for its ability to form coordination complexes with metal ions. This makes it a candidate for applications in various fields, including biochemical assays.
  • Potential Applications: Hydroxamic acids are often investigated for their antimicrobial and anticancer activities. Research suggests that compounds similar to 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid could potentially inhibit certain enzymes, which could be valuable in designing therapeutic agents.
  • Complex Structure: The presence of multiple substituents on the phenyl ring adds complexity and may influence the compound's biological activity. The intriguing arrangement of butoxy and methoxy groups can alter the electronic properties of the molecule.
  • Research Potential: Ongoing research in the field aims to explore and optimize compounds like this one, focusing on modifying its structure for improved efficacy and reduced side effects. As researchers delve deeper into structure-activity relationships, this compound could serve as a significant model.
  • Nature-Inspired Design: The intricate design of this molecule is inspired by natural products and enzyme mechanisms, showcasing the interplay between synthetic chemistry and biological functions.

In summary, 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid stands out as a prime example of how structural modifications can synergize to create compounds with potential therapeutic applications. Its study not only expands our understanding of hydroxamic acids but also inspires the continued exploration of novel chemical entities in drug discovery.

ADVERTISEMENT