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Bromoclorodione

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Identification
Molecular formula
C6HBr2ClNO
CAS number
532-91-2
IUPAC name
2,6-dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one
State
State
At room temperature, the compound is typically found in a solid crystalline state. The solid nature is attributed to the compound's molecular structure, which is dense and compact due to the presence of heavy halogen atoms.
Melting point (Celsius)
115.30
Melting point (Kelvin)
388.45
Boiling point (Celsius)
326.70
Boiling point (Kelvin)
599.85
General information
Molecular weight
315.35g/mol
Molar mass
315.3460g/mol
Density
3.1670g/cm3
Appearence

2,6-Dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one appears as a crystalline solid with distinct coloring due to its chemical structure. The presence of bromine and chlorine atoms imparts a certain halogenated aroma, and the crystals can exhibit various shades ranging from pale to more intense hues depending on the conditions of crystallization and purity.

Comment on solubility

Solubility of 2,6-dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one

The solubility of 2,6-dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one is influenced by its unique molecular structure, which incorporates multiple halogen substituents. This characteristic can significantly impact its solubility in various solvents.

Key points regarding its solubility include:

  • Polar vs. Nonpolar Solvents: The presence of both bromine and chlorine atoms tends to enhance solubility in polar solvents, while the larger cyclohexadiene structure may hinder solubility in nonpolar solvents.
  • Hydrogen Bonding: The imino group may facilitate hydrogen bonding with solvents, potentially increasing solubility in polar protic solvents like water.
  • Temperature Effects: Increasing temperature may improve solubility, allowing more of the compound to dissolve by increasing molecular motion.
  • Concentration Dependence: As with many organic compounds, solubility can vary with concentration, where saturation limits might inhibit further dissolution.

Though detailed experimental data on the solubility of this compound in specific solvents is limited, general trends suggest a nuanced solubility profile influenced by both the structural features and the solvent environment. As always, consulting experimental data for precise solubility measurements is recommended.

Interesting facts

Interesting Facts about 2,6-Dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one

This compound, 2,6-dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one, is an intriguing example of a halogenated organic compound. Its structural features lead to a variety of fascinating properties and potential applications. Here are some interesting aspects of this compound:

  • Halogenated Structure: The presence of bromine and chlorine atoms introduces unique reactivity patterns, making it a candidate for various chemical transformations.
  • Potential Biological Activity: Compounds like this are sometimes explored for their biological properties. It’s possible that they exhibit antimicrobial or antifungal activities, contributing to the development of new pharmaceuticals.
  • Stability Considerations: The stability of the imino group in the structure can influence the compound's reactivity and behavior in different environments, leading to potential applications in materials science.
  • Use in Synthesis: This compound may serve as an intermediate in organic synthesis, particularly in the creation of dyes or other functional materials due to its unique electronic properties.
  • Environmental Impact: Understanding the fate of halogenated compounds in the environment is crucial, as their stability can lead to bioaccumulation. Research into their degradation products is essential for assessing their ecological impact.

The study of compounds like 2,6-dibromo-4-chloroimino-cyclohexa-2,5-dien-1-one not only enhances our understanding of organic chemistry but also opens avenues for innovative applications in various fields. As scientists continue to explore the functionalities of such compounds, the possibilities for their use expand, showcasing the intricate relationship between molecular structure and chemical behavior.

Synonyms
537-45-1
2,6-Dibromoquinone-4-chloroimide
2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone
BQC reagent
2,6-Dibromoquinone-4-chlorimide
2,5-Cyclohexadien-1-one, 2,6-dibromo-4-(chloroimino)-
2,6-Dibromoquinone chlorimide
2,6-Dibromoquinone chloroimide
2,6-Dibromoquinone chloroimine
N-Chloro-2,6-dibromoquinoneimine
NSC 528
2,6-Dibromo-p-benzoquinone-4-chlorimine
2,6-Dibromoquinone 4-chlorimide
2,6-Dibromo-N-chloro-p-benzoquinoneimine
EINECS 208-667-1
2,6-Dibromo-4-(chloroimino)-2,5-cyclohexadien-1-one
BRN 2094249
H750J4PI0N
4-Chloroimino-2,6-dibromo-2,5-cyclohexadiene-1-one
AI3-51570
NSC-528
2,5-Cyclohexadien-1-one, 4-chloroimino-2,6-dibromo-
DTXSID1060215
4-07-00-02086 (Beilstein Handbook Reference)
2,6-DIBROMO-N-CHLOROQUINONIMINE
2,6-DIBROMOQUINONE-4-CHLORIMIDE [MI]
2,6-DBQC
DTXCID4041492
2,6-dibromo-4-chloroiminocyclohexa-2,5-dien-1-one
2,6-DIBROMOQUINONECHLOROIMIDE
C6H2Br2ClNO
UNII-H750J4PI0N
2,6-Dibromo-1,4-quinone-4-chlorimide
NSC528
SCHEMBL1683186
CHEMBL3276933
2,6-Dibromoquinone-4-chloroimine
2, 4-chloroimino-2,6-dibromo-
WLN: L6V DYJ BE DUNG FE
AAA53745
2, 2,6-dibromo-4-(chloroimino)-
AKOS015917283
CS-W012138
HY-W011422
PD088735
DB-052392
NS00022328
A829758
2,6-dibromo-4-chloroimino-1-cyclohexa-2,5-dienone
2,6-dibromo-4-(chloroimino)cyclohexa-2,5-dien-1-one
2,6-Dibromoquinone-4-chloroimide, JIS special grade
Q27279725
2,6-Dibromo-4-(chloroimino)-2,5-cyclohexadien-1-one #
2,6-bis(bromanyl)-4-chloranylimino-cyclohexa-2,5-dien-1-one