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2-Bromodibenzofuran

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Identification
Molecular formula
C12H7BrO
CAS number
3245-62-9
IUPAC name
2-bromodibenzofuran
State
State

At room temperature, 2-Bromodibenzofuran exists as a solid. It remains stable under normal conditions but should be stored in a cool, dry place to prevent degradation or reaction with environmental moisture.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
249.09g/mol
Molar mass
249.0940g/mol
Density
1.5778g/cm3
Appearence

2-Bromodibenzofuran appears as a white or off-white crystalline solid. Its purity and form can slightly alter its hue, potentially giving it a more beige or pale yellow tint due to impurities or exposure to light and air.

Comment on solubility

Solubility of 2-bromodibenzofuran

2-bromodibenzofuran, a compound with intriguing properties, exhibits distinct solubility characteristics influenced by its molecular structure. The solubility of this compound can be discussed in the context of several factors:

  • Polarity: The presence of the bromine atom adds a certain degree of polarity to the molecule, potentially enhancing its solvation in polar solvents.
  • Solvent Choice: 2-bromodibenzofuran is more soluble in organic solvents such as ethanol, acetone, and chloroform compared to polar solvents like water.
  • Temperature Dependency: As with many organic compounds, solubility can increase with temperature, allowing more of the compound to dissolve at elevated temperatures.
  • Hydrophobic Character: The dibenzofuran structure contributes to its hydrophobic nature, making it generally insoluble in water.

In conclusion, the solubility behaviors of 2-bromodibenzofuran are notably influenced by its molecular design and the types of solvents employed. Understanding these nuances is essential for applications in various fields, including organic synthesis and environmental studies.

Interesting facts

Interesting Facts About 2-Bromodibenzofuran

2-Bromodibenzofuran is a fascinating compound that has gained attention in the field of organic chemistry due to its unique structure and various applications. Here are some engaging insights about this intriguing compound:

  • Structural Significance: 2-Bromodibenzofuran features a fusion of a dibenzofuran structure with a bromine substituent. This configuration leads to interesting stereochemical properties and reactivity patterns.
  • Reactivity: The presence of the bromine atom at the 2-position can significantly influence the compound's behavior in chemical reactions. It can participate in nucleophilic substitutions, leading to further functionalization of the compound.
  • Applications in Synthesis: This compound acts as a useful building block in the synthesis of more complex molecules. Its unique structure can be exploited in the creation of natural products, pharmaceuticals, and advanced materials.
  • Importance in Research: Researchers have utilized 2-bromodibenzofuran in studies regarding molecular interaction and photophysics, helping to shed light on its potential in optoelectronic applications.

Overall, studying 2-bromodibenzofuran not only enhances our understanding of organic compounds but also opens avenues for innovative research and application in numerous fields. As one exploration into the world of aromatic compounds, it exemplifies the beauty and complexity associated with chemical substances.


Synonyms
2-Bromodibenzo[b,d]furan
86-76-0
2-BROMODIBENZOFURAN
2-BROMO-DIBENZOFURAN
Dibenzofuran, 2-bromo-
NSC 1735
MFCD00092338
C36TC73SME
DTXSID20235337
NSC-1735
2-Bromodibenzo(b,D)furan
4-bromo-8-oxatricyclo(7.4.0.02,7)trideca-1(13),2,4,6,9,11-hexaene
4-bromo-8-oxatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
NSC1735
2-Bromo dibenzofuran
Dibenzofuran, 2-bromo- (8CI)(9CI)
UNII-C36TC73SME
SCHEMBL67700
2-Bromo-dibenzofuran, 98%
Dibenzofuran, 2-bromo-(8CI)
DTXCID20157828
Dibenzofuran, 2-bromo-(8CI)(9CI)
AKOS000202592
CS-W014116
DS-2081
SB66894
SY033174
DB-056951
B4459
NS00120797
EN300-212013
4-bromo-8-oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaene
4-bromo-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),2,4,6,9,11-hexaene
659-733-5