Skip to main content

(7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate

ADVERTISEMENT
Identification
Molecular formula
C19H14N2O5
CAS number
144596-78-5
IUPAC name
(7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate
State
State

The compound is a solid at room temperature and due to its crystalline structure, it is often stable and well-defined under standard conditions.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
469.00
Boiling point (Kelvin)
742.15
General information
Molecular weight
365.33g/mol
Molar mass
365.3480g/mol
Density
1.4120g/cm3
Appearence

(7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate is often found in crystalline solid form, appearing as yellow or orange crystals. This compound is characteristically vibrant due to the presence of the nitro group that contributes to its hue.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate

(7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate is a chemical compound whose solubility can be influenced by several factors, including its molecular structure and the solvents in which it is tested.

Generally, this compound displays the following solubility characteristics:

  • Solvent Dependence: It tends to be soluble in organic solvents such as ethanol, acetone, and DMSO, due to its organic nature.
  • Water Solubility: The compound has limited solubility in water, which can be attributed to the presence of its aromatic and nitro groups that hinder hydrogen bonding.
  • pH Influence: The solubility may also vary with pH; basic conditions can enhance solubility through deprotonation of functional groups, whereas acidic environments may lead to decreased solubility.

As a general observation, chemicals with similar structural features often adhere to the principle of "like dissolves like," indicating that polar compounds dissolve well in polar solvents, while non-polar compounds prefer non-polar solvents.

In summary, understanding the solubility of (7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate is crucial for its application in various areas, and proper solvent selection is key to optimizing its use.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate

(7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate is a fascinating compound that belongs to the class of quinoline derivatives, widely recognized for their biological and chemical significance. This particular compound has sparked interest in various fields due to its complex structure and potential applications. Here are some key aspects:

  • Biological Activity: Quinoline derivatives are known for their varied biological properties, including antimicrobial, antimalarial, and anticancer activities. For instance, the nitro group in this compound is often implicated in enhancing such biological activities.
  • Synthetic Pathways: The synthesis of quinoline-based compounds typically involves innovative strategies, including cyclization reactions, which highlight the creativity and versatility of organic chemistry. The incorporation of methoxy groups can further improve solubility and bioavailability, making synthetic methods a focal area for research.
  • Potential Applications: This compound may serve as a lead structure for developing new pharmaceuticals and agrochemicals, contributing to advances in medicinal chemistry and agricultural sciences.
  • Structure-Activity Relationships (SAR): Understanding how variations in the structure of this compound affect its biological activity is essential for researchers. The presence of the 2-methoxyphenyl moiety can influence interaction with biological targets, exemplifying the significance of SAR studies.
  • Research Interest: The unique structural characteristics of (7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate make it a subject of interest in both academic research and pharmaceutical development, showcasing its relevance in tackling modern challenges in healthcare.

With ongoing research into its properties and potential uses, the implications of (7-nitro-8-quinolyl) 3-(2-methoxyphenyl)prop-2-enoate continue to unfold, making it a compelling topic for chemists and biochemists alike. As stated by renowned chemist Marie Curie, "I was taught that the way of progress was neither swift nor easy." This compound exemplifies the intricate balance between challenge and innovation in scientific exploration.