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(7-nitro-8-quinolyl) 3,4-dichlorobenzoate

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Identification
Molecular formula
C16H8Cl2N2O4
CAS number
216343-63-6
IUPAC name
(7-nitro-8-quinolyl) 3,4-dichlorobenzoate
State
State

At room temperature, (7-nitro-8-quinolyl) 3,4-dichlorobenzoate is a solid. This state is common for many organic compounds, particularly those with multiple aromatic rings and substituents like nitro and chloro groups.

Melting point (Celsius)
176.00
Melting point (Kelvin)
449.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
396.15g/mol
Molar mass
396.1930g/mol
Density
1.6200g/cm3
Appearence

This compound is typically a solid crystalline material. The crystals may appear as yellow to orange-yellow in color. The vibrant color is due to the nitro group, which is often responsible for such hues in organic compounds.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3,4-dichlorobenzoate

The solubility of (7-nitro-8-quinolyl) 3,4-dichlorobenzoate can be influenced by various factors, including its molecular structure and the polarity of the solvent used. Here are some key points to consider regarding its solubility:

  • Polarity: The presence of the nitro group and the quinoline structure contributes to polarity, which may affect its solubility in polar solvents.
  • Solvent Interaction: It is often more soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol than in water due to the hydrophobic nature of the aromatic rings.
  • Temperature Dependency: Solubility may increase with temperature, a common trend for many organic compounds.
  • pH Effects: The solubility might also vary with pH, especially if the compound has functional groups that can ionize, affecting its interaction with solvent molecules.

As a general rule, it is helpful to refer to the solubility data provided in specific experimental conditions, keeping in mind that "like dissolves like." Thus, a careful choice of solvent plays a crucial role in maximizing the solubility of (7-nitro-8-quinolyl) 3,4-dichlorobenzoate for practical applications.

Interesting facts

Exploring (7-nitro-8-quinolyl) 3,4-dichlorobenzoate

(7-nitro-8-quinolyl) 3,4-dichlorobenzoate is a fascinating compound that attracts attention in various fields of research, particularly in medicinal chemistry and materials science. Here are some key facts that amplify its significance:

  • Aromatic Amine Connections: This compound contains a quinoline structure, characterized by a fused ring system that contributes to its unique chemical properties.
  • Bioactivity: Compounds related to quinolines have been extensively studied for their potential biological activities, including antibacterial, antifungal, and antimalarial properties. This makes (7-nitro-8-quinolyl) 3,4-dichlorobenzoate an exciting candidate for further investigation in drug development.
  • Functional Group Diversity: As a derivative of benzoate, this compound showcases the versatility of functional groups, allowing for a variety of chemical reactions and transformations.
  • Fluorescent Properties: Many quinoline derivatives exhibit fluorescent properties, which could be leveraged in applications like organic light-emitting diodes (OLEDs) and fluorescent probes in biological imaging.

As noted by researchers, “The structural diversity presented by modifications on quinolines leads to a vast array of potential applications, from pharmaceuticals to optoelectronic materials.” This highlights the compound's potential impact across multiple scientific disciplines.

In summary, (7-nitro-8-quinolyl) 3,4-dichlorobenzoate is not just a chemical entity; it embodies a wealth of possibilities for innovation and discovery in the realms of chemistry and beyond.

Synonyms
BRN 1550763
BENZOIC ACID, 3,4-DICHLORO-, 7-NITRO-8-QUINOLYL ESTER
8-Quinolinol, 7-nitro-, 3,4-dichlorobenzoate
29007-10-1
3,4-Dichlorobenzoic acid 7-nitro-8-quinolyl ester
DTXSID50183231
RefChem:327017
DTXCID60105722
SCHEMBL4461811