7-Nitro-8-quinolyl 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate

Identification

Molecular formula

C₁₉H₁₄N₂O₅

CAS number

426473-66-8

IUPAC name

(7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate

State

At room temperature, it is a solid with a stable crystalline structure.

Melting point (Celsius)

157.50

Melting point (Kelvin)

430.65

Boiling point (Celsius)

327.80

Boiling point (Kelvin)

600.95

General information

Molecular weight

407.40g/mol

Molar mass

407.3960g/mol

Density

1.3220g/cm³

Appearence

The compound is typically observed as a yellow solid. It is aromatic with distinct crystalline properties, often forming needle-like crystals.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate

The solubility of (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate is a noteworthy aspect when considering its behavior in various solvents. Factors influencing solubility include:

Polarity of the Solvent: Polar solvents such as water may have limited interaction with this compound due to its relatively nonpolar characteristics.
Temperature: Solubility often increases with temperature, which may allow for greater dispersion in organic solvents.
Interactions with Functional Groups: The presence of methoxy and nitro groups suggests potential for hydrogen bonding, impacting solubility in more polar organic solvents.

It is important to note that the compound may exhibit varying solubility in different organic solvents, such as:

Dimethyl sulfoxide (DMSO) — often well-received for solubility of organic compounds
Ethyl acetate — a common solvent for various organic esters, which may aid its dissolution
Chloroform — frequently used for dissolving compounds with aromatic rings.

Understanding the solubility profile of (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate is essential for its practical applications in the fields of chemistry and pharmaceuticals. As with many complex chemical compounds, the solubility characteristics play a critical role in reactivity and usability.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate

(7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate is a compound that showcases the fascinating intersection of organic chemistry and medicinal applications. This compound is particularly noteworthy for the following reasons:

Versatile Applications: Its unique structure suggests potential applications in pharmacology, particularly in drug synthesis and development.
Quinoline Framework: The presence of the quinoline moiety in the structure has been associated with various biological activities, including anti-inflammatory and antimicrobial properties.
High Reactivity: The unsaturated ester functionality in this compound offers opportunities for further chemical modifications, making it a valuable intermediate in organic synthesis.

As a compound that bridges the gap between theory and practical application, (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate reflects the creativity and innovation found in modern chemistry research. Its synthesis may involve multiple steps, allowing for the exploration of reaction mechanisms and synthetic pathways.

Furthermore, research into this compound could unveil new insights into:

Drug Discovery: Studying its biological effects could inspire new therapeutic agents.
Environmental Chemistry: Investigating the compound's stability and degradation could contribute to understanding its environmental impact.
Structure-Activity Relationship: Examining how variations of its structure affect biological activity could lead to optimized compounds.

In summary, (7-nitro-8-quinolyl) 3-(4-methoxyphenyl)-2-methyl-prop-2-enoate is a compound worth exploring for its diverse applications and the rich chemistry it embodies. As emphasized in the field, "Every compound tells a story," and this compound is no exception!