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Bromoxylene

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Identification
Molecular formula
C7H6Br2
CAS number
n/a
IUPAC name
1,2-dibromo-3-methyl-benzene;1,2-dibromo-4-methyl-benzene;1,3-dibromo-2-methyl-benzene;1,3-dibromo-5-methyl-benzene;1,4-dibromo-2-methyl-benzene
State
State

At room temperature, Bromoxylene is in a liquid state.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
234.00
Boiling point (Kelvin)
507.15
General information
Molecular weight
249.94g/mol
Molar mass
249.9390g/mol
Density
1.8752g/cm3
Appearence

Bromoxylene typically appears as a colorless to pale yellow liquid. It is clear and has a distinctive aromatic odor characteristic of brominated aromatic compounds.

Comment on solubility

Solubility of 1,2-dibromo-3-methyl-benzene and Related Compounds

The solubility of brominated aromatic compounds, such as 1,2-dibromo-3-methyl-benzene, 1,2-dibromo-4-methyl-benzene, 1,3-dibromo-2-methyl-benzene, 1,3-dibromo-5-methyl-benzene, and 1,4-dibromo-2-methyl-benzene, can often be characterized as low in polar solvents but more favorable in non-polar solvents. This is largely due to their hydrophobic characteristics attributed to the bromine substituents and the aromatic ring.

Factors Influencing Solubility

When examining the solubility of these compounds, consider the following factors:

  • Molecular Structure: The presence of multiple bromine atoms increases molecular weight and may affect the overall strength of intermolecular forces.
  • Hydrophobicity: The non-polar character of the benzene ring tends to lead to low solubility in water, while enhancing solubility in organic solvents like hexane.
  • Substituent Position: Variations in the position of the methyl and bromine groups can slightly alter the solubility properties, although differences may not be highly significant.

General Solubility Trends

The following trends can generally be observed:

  • In water: Poorly soluble due to strong hydrogen bonding preference of water molecules over weak interactions with the brominated compounds.
  • In organic solvents: Much higher solubility, especially in non-polar solvents, due to favorable interactions.

In summary, while these dibromo-methyl benzenes exhibit low solubility in polar environments, they demonstrate a much more favorable solubility in non-polar solvents, making them important candidates in various applications within organic chemistry.

Interesting facts

Interesting Facts About 1,2-Dibromo-3-Methyl-Benzene

The compound 1,2-dibromo-3-methyl-benzene, also known as pseudocumene bromide, showcases the fascinating chemistry of halogenated aromatics. This compound features not just one, but two bromine atoms substituted on the benzene ring, which significantly alters its chemical properties and reactivity. Here are some noteworthy details:

  • Substitution Patterns: The position of the bromine atoms and methyl group plays a critical role in determining the reactivity and physical properties of the molecule. This structural diversity leads to varied applications in organic synthesis.
  • Applications: Compounds like 1,2-dibromo-3-methyl-benzene are used in various fields, including pharmaceuticals and agrochemicals, where they serve as intermediates in the synthesis of more complex molecules.
  • Environmental Impact: Considering halogenated compounds, studies frequently examine their environmental behavior and potential for bioaccumulation, raising questions about their safety and disposal.

Understanding the chemistry behind compounds such as 1,2-dibromo-3-methyl-benzene equips chemists with the tools to innovate, facilitating discoveries in both academia and industry.


Interesting Facts About 1,2-Dibromo-4-Methyl-Benzene

1,2-dibromo-4-methyl-benzene, commonly referenced as p-xylene dibromide, is another intriguing compound in the realm of halogenated aromatic hydrocarbons. Its unique structure leads to a variety of interesting characteristics:

  • Stereoelectronic Effects: The presence of bromine atoms and the methyl group in specific arrangements can result in significant electronic effects that impact the stability and reactivity of the compound.
  • Biological Activity: Some studies suggest that brominated aromatic compounds exhibit different levels of biological activity, which could lead to potential pharmaceutical applications revolving around drug design.
  • Reactivity: The compound can undergo electrophilic substitution reactions, opening the door to further functionalization and complex synthesis pathways.

Researchers are continuously exploring the properties of compounds like 1,2-dibromo-4-methyl-benzene, contributing to advancements in materials science and medicinal chemistry.


Interesting Facts About 1,3-Dibromo-2-Methyl-Benzene

The compound 1,3-dibromo-2-methyl-benzene, also known as 2-methyl-1,3-dibromobenzene, stands out in the study of aromatic bromides due to its unique application possibilities:

  • Structural Variance: Like its counterparts, the position of halogen substitution significantly affects the compound’s reactivity, which chemists can leverage for organic transformations.
  • Synthetic Pathways: This compound offers a rich template for the development of broader chemical hierarchies, which could pave the way for synthetic methods in complex organic synthesis.
  • Research Applications: Its unique bromination and methyl substitution patterns invite exploration in various chemical reactions, intertwining studies of kinetic effects and thermodynamic stabilities.

The synthesis and study of 1,3-dibromo-2-methyl-benzene provide valuable insights into the dynamic world of organic chemistry.


Interesting Facts About 1,3-Dibromo-5-Methyl-Benzene

1,3-dibromo-5-methyl-benzene, often noted as 5-methyl-1,3-dibromobenzene, is a compelling subject for organic chemists due to its versatile properties:

  • Functionalization Potential: The presence of both bromine substituents and the methyl group opens wide-reaching possibilities for further chemical reactions, particularly in electrophilic aromatic substitution.
  • Chemical Behavior: Analyzing the sterics and electronics associated with this compound helps researchers develop more efficient synthetic strategies influenced by its unique behavior.
  • Industrial Relevance: Compounds like 1,3-dibromo-5-methyl-benzene find applications in the formulation of specialty chemicals and materials, emphasizing their industrial relevance.

The ongoing exploration of 1,3-dibromo-5-methyl-benzene enriches our understanding of halogenated compounds and their multifaceted roles in chemical synthesis.


Interesting Facts About 1,4-Dibromo-2-Methyl-Benzene

1,4-dibromo-2-methyl-benzene, known as 2-methyl-1,4-dibromobenzene, captivates chemists with its distinct substitution pattern leading to diverse chemistry:

  • Balanced Structure: The symmetrical arrangement of bromine atoms significantly influences how the compound participates in substitution reactions, making it a prime candidate for various organic transformations.
  • Material Science: Similar halogenated compounds are being studied for incorporation into polymers and materials, where their properties are tailored for specific applications.
  • Health and Safety: As with many brominated compounds, researchers are investigating potential health implications, ensuring safe handling and use in industrial processes.

Investigation into compounds like 1,4-dibromo-2-methyl-benzene not only advances organic synthesis but also emphasizes the importance of understanding chemical safety and environmental stewardship.