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6-Bromo-1,2-naphthoquinone

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Identification
Molecular formula
C10H5BrO2
CAS number
571-94-0
IUPAC name
6-bromonaphthalene-1,2-dione
State
State

6-Bromo-1,2-naphthoquinone is typically found under normal conditions as a crystalline solid. It is usually handled at room temperature in experiments and storage conditions.

Melting point (Celsius)
119.00
Melting point (Kelvin)
392.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
237.05g/mol
Molar mass
237.0310g/mol
Density
1.7440g/cm3
Appearence

6-Bromo-1,2-naphthoquinone is typically a solid compound. It has a characteristic intense yellow or orange to brown coloration in its pure form. This coloration is due to the presence of the conjugated quinone structure in the molecule.

Comment on solubility

Solubility of 6-bromonaphthalene-1,2-dione

6-bromonaphthalene-1,2-dione, with its intricate molecular structure, exhibits unique solubility characteristics that are important for various applications. Typically, this compound is described as being:

  • Moderately soluble in organic solvents such as ethanol and chloroform.
  • Poorly soluble in water due to its non-polar nature and substantial aromatic character.

This limited solubility in aqueous solutions may be attributed to:

  1. The presence of bromine substituents, which influence polarity.
  2. The central dione structure which enhances intermolecular interactions in non-polar solvents.

In practical terms, this means that researchers and chemists may often prefer to use organic solvents when working with 6-bromonaphthalene-1,2-dione for dissolving or reacting it in various chemical processes. As with many aromatic compounds, the solubility can significantly affect its reactivity and interaction with other chemical species.

Overall, understanding the solubility traits of 6-bromonaphthalene-1,2-dione is crucial for optimizing its usage in chemical synthesis and industrial applications.

Interesting facts

Interesting Facts about 6-Bromonaphthalene-1,2-Dione

6-Bromonaphthalene-1,2-dione is a fascinating compound in the field of organic chemistry. It belongs to the class of naphthoquinones, which are interesting due to their structural complexity and biological significance. Here are some noteworthy aspects of this compound:

  • Structural Significance: This compound features a naphthalene ring system with two carbonyl groups. The substitution of a bromine atom enhances both its chemical reactivity and versatility in synthetic applications.
  • Biological Activity: Compounds derived from naphthoquinones, including 6-bromonaphthalene-1,2-dione, are known to exhibit a range of biological activities. They have shown promise as antimicrobial and anticancer agents in various studies.
  • Synthetic Applications: The compound can serve as a valuable intermediate in the synthesis of more complex organic molecules. Its reactivity allows for further functionalization through various chemical reactions.
  • Research Potential: Ongoing research continues to explore the potential of naphthoquinone derivatives in material science, particularly in the development of organic semiconductors and dyes.

As Dr. Jane Goodall aptly put it, "Biochemistry is simply chemistry applied to living things." This rings true, especially with the unique properties and potential applications of 6-bromonaphthalene-1,2-dione at the intersection of organic chemistry and biological research.

This compound illustrates the importance of understanding chemical structures, as modifications can lead to vastly different chemical behaviors and activities. As scientists explore the myriad possibilities, the future looks promising for compounds like 6-bromonaphthalene-1,2-dione!

Synonyms
Bonaphthone
Bonafton
6-Bromo-1,2-naphthoquinone
Bonaphthon
6-BROMO-1,2-NAPHTHALENEDIONE
1,2-Naphthalenedione, 6-bromo-
6-Brom-1,2-naphthochinon
1,2-NAPHTHOQUINONE, 6-BROMO-
TX6H0Q18AM
NSC 37564
BRN 1944551
BROMNAPHTOQUINONE
NSC-37564
UNII-TX6H0Q18AM
DTXSID30219800
BROMNAPHTOQUINONE [WHO-DD]
4-07-00-02422 (Beilstein Handbook Reference)
UA 13082
DTXCID40142291
1,2-Naphthalenedione, 6-bromo-(9CI)
6-bromonaphthalene-1,2-dione
6954-48-9
6-bromo-1,2-dihydronaphthalene-1,2-dione
SCHEMBL2525185
CHEMBL4303595
MXWZRRPNVLCHMY-UHFFFAOYSA-N
BDBM442806
ALBB-014892
NSC37564
MFCD00464116
STK028617
AKOS001632647
HY-W269306
LS-04730
DB-317968
CS-0314608
EU-0038136
H30918
CS-004/04003052
BRD-K34149328-001-01-3
BRD-K34149328-001-02-1