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(7-nitro-8-quinolyl) 3-bromobenzoate

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Identification
Molecular formula
C16H9BrN2O4
CAS number
211001-12-0
IUPAC name
(7-nitro-8-quinolyl) 3-bromobenzoate
State
State

At room temperature, (7-nitro-8-quinolyl) 3-bromobenzoate is typically found in a solid state. This solid form lends itself well to handling and storage under normal laboratory conditions.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
368.15g/mol
Molar mass
368.1220g/mol
Density
1.5400g/cm3
Appearence

The compound (7-nitro-8-quinolyl) 3-bromobenzoate typically appears as a crystalline solid. It may vary in color depending on the specific characteristics of the synthesis and any impurities present, but often appears as a light yellow or pale orange crystalline powder.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-bromobenzoate

The solubility of (7-nitro-8-quinolyl) 3-bromobenzoate can be quite complex, influenced by various factors such as temperature, solvent polarity, and the compound's molecular structure. Here are some key points to consider:

  • Solvent Compatibility: This compound tends to be more soluble in organic solvents like dimethyl sulfoxide (DMSO) and acetone than in water. This is due to its organic nature and the presence of aromatic rings.
  • Temperature Dependence: Solubility may increase with temperature; thus, warming the solvent can facilitate the dissolution process.
  • Polarity Influence: The solubility is also affected by the polarity of the solvent used. Polar solvents might not effectively dissolve the compound due to its non-polar aspects.

In general, evaluating the solubility of (7-nitro-8-quinolyl) 3-bromobenzoate involves understanding its interaction with different solvents. Experimentation is often required to determine the exact solubility limits under various conditions.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 3-bromobenzoate

(7-nitro-8-quinolyl) 3-bromobenzoate is a fascinating compound that boasts a unique structural configuration, making it significant in various fields of chemistry.

  • Biological Activity: This compound has exhibited notable biological activities, particularly as a potential pharmacological agent. Its structural features allow it to interact with biological systems effectively.
  • Fluorescence Properties: Compounds like (7-nitro-8-quinolyl) 3-bromobenzoate are known for their fluorescence properties, which can be harnessed in applications such as fluorescence microscopy or as a tracer in biological assays.
  • Application in Proton Sensors: The incorporation of a quinoline moiety makes it a candidate for innovative sensor development, contributing to environmental monitoring and chemical detection methodologies.
  • Research Potential: Research studies are increasingly focusing on its derivatives, as modifying certain functional groups can lead to enhanced properties or novel uses.

In the words of a renowned chemist, "The beauty of organic chemistry lies in its ability to create compounds that have real-world applications." This sentiment perfectly captures the essence of (7-nitro-8-quinolyl) 3-bromobenzoate, as it bridges the gap between theoretical chemistry and practical application.

As a compound that embodies the intersection of organic synthesis and biological relevance, (7-nitro-8-quinolyl) 3-bromobenzoate serves as an exciting subject for ongoing research and exploration.

Synonyms
BENZOIC ACID, m-BROMO-, 7-NITRO-8-QUINOLYL ESTER
29007-06-5
BRN 1548656
8-Quinolinol, 7-nitro-, m-bromobenzoate
m-Bromobenzoic acid 7-nitro-8-quinolyl ester
SCHEMBL4470651
DTXSID60183227