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

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Identification
Molecular formula
C18H11ClNO4
CAS number
156887-81-9
IUPAC name
(7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate
State
State

At room temperature, this compound is in a solid state. It is typically stored under dry and cool conditions to prevent any degradation or reaction with moisture in the air.

Melting point (Celsius)
186.70
Melting point (Kelvin)
459.85
Boiling point (Celsius)
577.30
Boiling point (Kelvin)
850.45
General information
Molecular weight
382.82g/mol
Molar mass
382.8150g/mol
Density
1.3870g/cm3
Appearence

This compound typically appears as a crystalline powder which may have a yellowish color. The specific appearance can depend on the method of synthesis and purity level.

Comment on solubility

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

The solubility of (7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate can be influenced by several factors, leading to interesting behavior in various solvents. Understanding these solubility characteristics can greatly aid in applications or further research involving this compound.

Key Points Regarding Solubility:

  • Polar vs. Nonpolar Solvents: This compound tends to exhibit higher solubility in nonpolar organic solvents due to its aromatic and aliphatic characteristics.
  • Temperature Sensitivity: Increasing the temperature can generally enhance solubility, yet the exact temperature range may vary based on the specific solvent used.
  • pH Dependence: If dissolved in aqueous solutions, the solubility may be affected by changes in pH, particularly because it contains both nitro and aromatic groups which can interact with protons.

It is essential to remember that **"like dissolves like"**; hence, choosing the correct solvent for this compound is critical. In solvent selection, the balance between polarity and functional group interactions plays a significant role. Ultimately, experimenting with varying conditions will yield the most insightful data on solubility characteristics for (7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate.

Interesting facts

Interesting Facts About (7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate

(7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate, often referred to in scientific literature, presents several noteworthy characteristics that capture the attention of chemists and biochemists alike. This compound is primarily recognized for its role in various biological and chemical applications.

Applications and Uses

  • Antimicrobial Properties: The compound exhibits potential antimicrobial activity, making it a candidate for developing new pharmaceuticals.
  • Fluorescent Properties: Its unique structural features allow for applications in fluorescent labeling, which is significant in biochemical assays.
  • Research Tool: This compound is often utilized in research settings to study various biochemical pathways and mechanisms.

Structural Significance

The quinoline moiety is particularly important in medicinal chemistry. Quotably, "the inclusion of a nitro group can enhance the overall reactivity and selectivity of the compound." This highlights how small modifications can lead to significant changes in chemical behavior and interaction.

Safety and Handling

Like many chemical compounds, safety is of utmost importance when handling (7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate. Proper personal protective equipment (PPE) is essential, and conducting experiments in a well-ventilated area or fume hood is recommended. Attention to detail and safety protocols ensures successful and safe experimentation.

In conclusion, (7-nitro-8-quinolyl) 3-(4-chlorophenyl)prop-2-enoate is a compound rich with potential, bridging the gaps between chemistry, biology, and medicine. Its features invite ongoing research and exploration in various fields, promising to contribute to advancements in science and technology.