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5,7-Dibromo-2-benzoxazolinone

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Identification
Molecular formula
C7H3Br2NO2
CAS number
15252-59-8
IUPAC name
5,7-dibromo-3H-1,3-benzoxazol-2-one
State
State

The compound is a solid at room temperature.

Melting point (Celsius)
187.00
Melting point (Kelvin)
460.15
Boiling point (Celsius)
398.00
Boiling point (Kelvin)
671.15
General information
Molecular weight
280.90g/mol
Molar mass
280.9040g/mol
Density
2.3920g/cm3
Appearence

5,7-Dibromo-2-benzoxazolinone typically appears as a white to off-white crystalline powder. The crystals may have a slightly yellowish tint due to the bromine content. It is generally solid at room temperature, displaying a uniform texture conducive for use in various chemical reactions.

Comment on solubility

Solubility Characteristics of 5,7-Dibromo-3H-1,3-benzoxazol-2-one

The solubility of 5,7-dibromo-3H-1,3-benzoxazol-2-one can be influenced by several factors, including its molecular structure and the surrounding environment. Generally, this compound exhibits specific solubility traits that are noteworthy:

  • Solvent Dependence: The solubility is highly dependent on the solvent used. It tends to show better solubility in organic solvents such as dimethyl sulfoxide (DMSO) and acetone.
  • Polar vs. Non-Polar Solvents: In polar solvents, the compound may have limited solubility due to the hydrophobic characteristics imparted by the bromine substituents.
  • Temperature Influence: Increasing temperature can enhance solubility, which is a common trait for many organic compounds.

To summarize, while 5,7-dibromo-3H-1,3-benzoxazol-2-one may demonstrate variable solubility based on the chosen solvent, one could conclude that it is more suited for non-polar to slightly polar environments. Experimentation is essential to determine optimal conditions for dissolving this compound effectively.

Interesting facts

Exploring 5,7-Dibromo-3H-1,3-benzoxazol-2-one

5,7-Dibromo-3H-1,3-benzoxazol-2-one is a fascinating compound that merges the realms of organic chemistry and materials science. This compound, characterized by its unique structural features, has garnered interest due to several intriguing aspects:

  • Biological Activity: This compound belongs to a class known for potential biological activities. Research suggests that similar benzoxazole derivatives can exhibit antibacterial and antifungal properties, which makes them valuable in pharmaceutical applications.
  • Importance in Dye Chemistry: The benzoxazole moiety is often utilized in dye synthesis. The presence of bromine atoms can enhance dyeing properties and increase the stability of the resultant dye compounds.
  • Photophysical Properties: Compounds like 5,7-dibromo-3H-1,3-benzoxazol-2-one can demonstrate unique light absorption and emission spectra, making them interesting candidates for fluorescence studies and potential applications in sensors.
  • Potential Reactivity: The bromine substituents can act as reactive sites for further chemical modifications, opening doors for researchers to develop analogs with tailored properties for specific applications.
  • Environmental Interest: Compounds with similar structures are being investigated for their role in agricultural chemistry, particularly in the development of environmentally friendly pesticides.

In summary, 5,7-dibromo-3H-1,3-benzoxazol-2-one is not merely a compound of interest but a promising structure that invites further exploration and research. Its potential applications extend across various fields, from pharmaceuticals to materials science.

Synonyms
5459-02-9
2-BENZOXAZOLINONE, 5,7-DIBROMO-
5,7-Dibromobenzoxazol-2(3H)-one
5,7-Dibromo-2-benzoxazolinone
5,7-dibromo-3H-1,3-benzoxazol-2-one
MHX3ZR3EY8
2(3H)-Benzoxazolone, 5,7-dibromo-
5,7-dibromobenzo[d]oxazol-2(3H)-one
NSC-25001
NSC25001
NSC 25001
BRN 0152969
UNII-MHX3ZR3EY8
2-Benzoxazolinone,7-dibromo-
SCHEMBL2149064
DTXSID40203018
2(3H)-Benzoxazolone,7-dibromo-
AGSLHFQPWVSWHT-UHFFFAOYSA-N
5,7-dibromo-1,3-benzoxazol-2(3H)-one
5,7-DIBROMO-2(3H)-BENZOXAZOLONE
DB-087340