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

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Identification
Molecular formula
C18H11ClNO4
CAS number
216644-57-2
IUPAC name
(7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate
State
State

At room temperature, (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate is typically a solid. It is not volatile and is stable under normal conditions. Handling should be done in well-ventilated areas to avoid inhalation of dust, and it should be stored away from light to prevent degradation.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
652.15
Boiling point (Kelvin)
925.30
General information
Molecular weight
353.74g/mol
Molar mass
353.7600g/mol
Density
1.4200g/cm3
Appearence

This compound typically appears as a crystalline powder. It may have a yellow to orange color due to the presence of the nitro and quinoline groups. The exact shade can vary depending on purity and particle size.

Comment on solubility

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

The solubility of (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate can be influenced by various factors such as temperature, polarity, and the presence of solvents. Generally, compounds of this nature may exhibit the following solubility characteristics:

  • Polar Solvents: This compound may show limited solubility in polar solvents like water, due to its relatively large organic structure.
  • Non-Polar Solvents: It is likely to be more soluble in non-polar solvents such as hexane or chloroform, where the organic components can interact more favorably.
  • Temperature Dependence: Like many organic compounds, solubility can increase with temperature, making the compound more soluble in hot solvents than in cold.

Overall, while specific solubility data for (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate may not be extensively documented, the trends suggest that careful consideration of solvent choice and experimental conditions will be essential to effectively dissolve this compound in a laboratory setting.

In summary, understanding the solubility of organic compounds like (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate relies on:

  1. Analyzing molecular interactions
  2. Considering environmental factors
  3. Testing various solvents to optimize dissolution

By taking these aspects into account, researchers can better predict and manipulate the solubility of this intriguing compound.

Interesting facts

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

(7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate is a fascinating compound with a variety of applications and characteristics that make it worthy of study. Here are some compelling points to consider:

  • Structurally Unique: This compound features a quinoline ring, which is known for its role in the synthesis of various bioactive molecules. The presence of a nitro group at position 7 enhances its reactivity.
  • Pharmacological Potential: Compounds containing the quinoline and chlorophenyl moieties are often explored for their medicinal properties, including antimicrobial and antitumor activities. This particular compound could potentially contribute to new therapeutic agents.
  • Mechanistic Studies: As a scientist, one might be interested in how this compound interacts at a molecular level. Understanding its mechanism of action could reveal insights into drug design and development.
  • Versatile Chemistry: (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate can participate in various chemical reactions, including electrophilic substitutions and nucleophilic additions, making it a valuable intermediate for synthetic organic chemistry.
  • Environmental Implications: Studying the degradation and environmental impact of such compounds is crucial. The interactions of chlorinated compounds with natural systems can lead to the formation of potentially harmful byproducts.
  • Historical Significance: Quinoline derivatives have been historically significant in medicinal chemistry due to their diverse pharmacological effects, with some being used as anti-malarial drugs in the past.

In summary, (7-nitro-8-quinolyl) 3-(2-chlorophenyl)prop-2-enoate stands out due to its potential pharmaceutical applications and interesting structural features. Its role in organic synthesis and the exploration of its biological effects can foster new discoveries in the field of medicinal chemistry.