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

Identification

Molecular formula

C₂₀H₁₂Cl₂N₂O₄

CAS number

93479-60-8

IUPAC name

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

State

This compound is typically a solid at room temperature, exhibiting its distinctive crystalline structure.

Melting point (Celsius)

102.00

Melting point (Kelvin)

375.15

Boiling point (Celsius)

235.00

Boiling point (Kelvin)

508.15

General information

Molecular weight

402.23g/mol

Molar mass

402.1900g/mol

Density

1.4500g/cm³

Appearence

The compound appears as a crystalline solid with a pale to bright yellow coloration due to the presence of the nitro group which often imparts such color characteristics.

Comment on solubility

Solubility Characteristics of (7-nitro-8-quinolyl) 3-(3,4-dichlorophenyl)-2-methyl-prop-2-enoate

The solubility of (7-nitro-8-quinolyl) 3-(3,4-dichlorophenyl)-2-methyl-prop-2-enoate showcases some intriguing properties, reflecting its unique molecular structure. This compound, characterized by both its quinoline and prop-2-enoate moieties, presents a complex interaction with solvents. Here are some key points regarding its solubility:

Polar Solvents: The presence of the nitro group can enhance solubility in polar solvents such as water and alcohols, but the overall solubility may still be limited.
Nonpolar Solvents: Given the presence of the dichlorophenyl group, this compound tends to show increased solubility in nonpolar solvents like chloroform or ether.
Temperature Dependency: Solubility may be significantly affected by temperature. Generally, higher temperatures improve solubility for many organic compounds.
Hydrophobic Effects: The bulky and hydrophobic groups present may hinder solubility in aqueous environments.

In practice, **understanding the solubility** of this compound is crucial, as it affects its bioavailability, applications in various solvents, and potential usage in pharmaceuticals. As highlighted, the interplay between its various functional groups creates a distinctive profile that necessitates careful consideration in experimental contexts.

Interesting facts

Exploring (7-nitro-8-quinolyl) 3-(3,4-dichlorophenyl)-2-methyl-prop-2-enoate

(7-nitro-8-quinolyl) 3-(3,4-dichlorophenyl)-2-methyl-prop-2-enoate is a fascinating compound that brings together unique structural features and potential applications.

Key Features

Diverse Applications: This compound is of interest in pharmaceutical research due to its potent effects and potential therapeutic uses.
Complex Structure: The combination of a quinolyl unit with a 3-(3,4-dichlorophenyl) moiety creates a compound with intriguing electronic properties.
Importance in Drug Development: The structural elements may influence its interactions with biological targets, making it a subject for medicinal chemistry studies.
Research Potential: The unique nitro group in the quinolyl ring may enhance its reactivity, opening avenues for the synthesis of novel derivatives.

According to some chemists, "The intricate balance of structure and function in such compounds exemplifies the beauty of medicinal chemistry." Understanding these interactions is crucial for discovering new drugs that effectively target diseases.

Interesting Aspects of the 7-Nitro-8-Quinoline Framework

This framework is often noted for its ability to:

Participate in electron transfer reactions, which are vital for various biological processes.
Act as a ligand that coordinates with metal ions, potentially influencing catalytic and therapeutic outcomes.
Facilitate the development of fluorescent probes, thanks to its aromatic system.

In conclusion, the multifaceted nature of (7-nitro-8-quinolyl) 3-(3,4-dichlorophenyl)-2-methyl-prop-2-enoate not only makes it a compound worth studying but also a gateway to new discoveries in the world of chemistry. Its potential implications in various fields continue to fuel research enthusiasm.