Skip to main content

1,3-Dibromo-2,4-dimethylbenzene

ADVERTISEMENT
Identification
Molecular formula
C8H8Br2
CAS number
25344-23-0
IUPAC name
1,3-dibromo-2,4-dimethyl-benzene
State
State

At room temperature, 1,3-dibromo-2,4-dimethylbenzene is in a solid state, typically as a crystalline substance. Its stability and appearance make it suitable for use in various industrial applications, particularly in organic synthesis.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.15
Boiling point (Celsius)
241.00
Boiling point (Kelvin)
514.15
General information
Molecular weight
261.96g/mol
Molar mass
261.9810g/mol
Density
1.6565g/cm3
Appearence

1,3-Dibromo-2,4-dimethylbenzene is typically a white to light yellow crystalline solid. It is often in the form of needles or crystalline powder, which can have a mild aromatic odor characteristic to brominated aromatic hydrocarbons.

Comment on solubility

Solubility of 1,3-Dibromo-2,4-dimethyl-benzene

1,3-Dibromo-2,4-dimethyl-benzene, also known as a brominated aromatic compound, exhibits interesting solubility characteristics that are largely influenced by its molecular structure. This compound is largely nonpolar due to the presence of the aromatic ring and the bromine substituents. As a result, it has limited solubility in polar solvents.

Key Points on Solubility:

  • Solvent Type: It is more soluble in nonpolar solvents such as hexane and toluene.
  • Polar Solvents: It shows poor solubility in polar solvents like water and alcohol.
  • Hydrophobic Interactions: The hydrophobic nature of the aromatic system contributes to its tendency to dissolve in organic solvents rather than aqueous environments.

In summary, the solubility of 1,3-dibromo-2,4-dimethyl-benzene can be succinctly concluded as follows: "Like dissolves like." The compound favors nonpolar environments, making it essential for applications that require solubility in organic media.

Interesting facts

Interesting Facts about 1,3-Dibromo-2,4-Dimethylbenzene

1,3-Dibromo-2,4-dimethylbenzene is a fascinating compound that belongs to the class of aromatic hydrocarbons. Its unique structure and reactivity make it a subject of interest in various fields of chemistry, including organic synthesis and materials science.

Chemical Structure

This compound features a benzene ring with two bromine atoms and two methyl groups, specifically positioned for distinct chemical properties. The bromine atoms make it a halogenated aromatic compound, which significantly influences its reactivity and potential applications.

Key Characteristics

  • Reactivity: The presence of bromine atoms introduces sites for electrophilic substitution reactions, making it a useful intermediate in synthetic organic chemistry.
  • Applications: It has potential uses in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.
  • Environmental Impact: Due to its brominated nature, it is essential to consider the environmental implications and toxicity associated with its synthesis and use.

Interesting Chemistry

In terms of its reactions, it can undergo various transformations, such as:

  • Nucleophilic substitution: where nucleophiles can replace bromine atoms, leading to diverse products.
  • Reduction: which can convert bromine groups to simpler substituents, thus modifying the compound's reactivity.

Quote from a Chemist: "1,3-Dibromo-2,4-dimethylbenzene serves as an excellent example of how small changes in molecular structure can lead to significant variations in chemical behavior." This encapsulates the essence of studying aromatic compounds and their derivatives.

Overall, 1,3-dibromo-2,4-dimethylbenzene is more than just a compound; it's a gateway to understanding complex organic reactions and real-world applications!

Synonyms
1,3-dibromo-2,4-dimethylbenzene
90434-19-8
DTXSID00275094
RefChem:218386
DTXCID60226542
2,4-Dibromo-m-xylene
MFCD11846009
Benzene, 1,3-dibromo-2,4-dimethyl-
1,3-dibromo-2,4-dimethyl-benzene
SCHEMBL3393490
SCHEMBL3396598
SCHEMBL30499370
2.4-Dibrom-1.3-dimethylbenzol
CK2331
AKOS015995440
AS-45887
SY239595
DB-078685
CS-0061133
EN300-2003030
F037661