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2-Bromo-4-methylphenol

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Identification
Molecular formula
C7H7BrO
CAS number
3964-55-6
IUPAC name
2-bromo-4-methyl-phenol
State
State
At room temperature, 2-Bromo-4-methylphenol is a solid.

It is often handled as a powder in laboratory settings and may be stored in a dry, cool environment to maintain its stability.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.15
Boiling point (Celsius)
279.00
Boiling point (Kelvin)
552.15
General information
Molecular weight
187.04g/mol
Molar mass
187.0410g/mol
Density
1.5270g/cm3
Appearence

2-Bromo-4-methylphenol is a crystalline solid that typically appears as a white to off-white powder. It may form translucent to opaque crystals, depending on purity and sample preparation.

Comment on solubility

Solubility of 2-bromo-4-methyl-phenol

2-bromo-4-methyl-phenol, with the chemical formula C7H8BrO, exhibits notable solubility characteristics that can be attributed to its molecular structure. Understanding its solubility helps in various applications, especially in organic synthesis and pharmaceuticals.

Key Points About Solubility:

  • Polarity: The presence of the -OH (hydroxyl) group contributes to the molecule's polarity, enhancing its ability to dissolve in polar solvents like water.
  • Nonpolar Solvents: Conversely, 2-bromo-4-methyl-phenol also displays some solubility in nonpolar solvents due to the hydrophobic nature of the aromatic ring.
  • Temperature Effects: Solubility can increase with temperature; thus, heating the solvent may facilitate dissolution.
  • Hydrogen Bonding: The hydroxyl group enables hydrogen bonding with solvent molecules, which is crucial for its solubility in polar solvents.

In summary, 2-bromo-4-methyl-phenol is generally more soluble in polar solvents while retaining some degree of compatibility with nonpolar environments. This dual solubility profile is essential for its functional applications in chemistry.

Interesting facts

Interesting Facts About 2-Bromo-4-methyl-phenol

2-Bromo-4-methyl-phenol, also known by its IUPAC name, is a fascinating compound that has garnered attention in both the chemical and pharmaceutical fields. Here are some key insights:

  • Applications in Medicine: This compound is often used as a precursor in the synthesis of various pharmaceuticals. It exhibits antimicrobial properties, making it a candidate for developing antiseptic agents.
  • Research Interest: Researchers have shown interest in its potential anti-inflammatory effects. By studying compounds like 2-bromo-4-methyl-phenol, scientists hope to unveil new treatments for inflammatory diseases.
  • Substituted Phenolic Compounds: As a member of the phenol family, this compound features substituents that significantly influence its reactivity and properties. The presence of the bromine and methyl groups affects the electron density around the aromatic ring, leading to unique chemical behaviors.
  • Environmental Impact: Although it has beneficial uses, it is crucial to consider the environmental impact of compounds like 2-bromo-4-methyl-phenol. Researchers are exploring the degradation and bioaccumulation aspects to ensure safety and sustainability.
  • Challenging Synthesis: The synthesis of this compound can be challenging due to the need for specific reaction conditions and careful handling of the bromine reagent. This presents an excellent learning opportunity for chemistry students.

In summary, 2-bromo-4-methyl-phenol is more than just a simple chemical compound; it embodies the intersection of science, health, and environmental studies. As the world of chemistry evolves, compounds like this play a crucial role in shaping future discoveries.

Synonyms
2-Bromo-4-methylphenol
6627-55-0
2-Bromo-p-cresol
Phenol, 2-bromo-4-methyl-
3-Bromo-4-hydroxytoluene
U7N9MXC7HG
EINECS 229-595-7
NSC 60115
BRN 1859036
NSC-60115
DTXSID8074574
4-06-00-02143 (Beilstein Handbook Reference)
DTXCID0044781
mtidygltaozogu-uhfffaoysa-n
2-bromo-4-methyl-phenol
p-CRESOL, 2-BROMO-
MFCD00002151
NSC60115
p-Cresol, 2-bromo- (6CI,7CI,8CI); 2-Bromo-4-methylphenol; 2-Bromo-4-cresol; 2-Bromo-p-cresol; 3-Bromo-4-hydroxytoluene; NSC 60115
UNII-U7N9MXC7HG
SCHEMBL358697
2-Bromo-4-methylphenol, 96%
AKOS000121426
CS-W016869
FB33955
HY-W016153
PB43240
PS-8466
AC-25967
SY049117
DB-020645
B0808
NS00035997
EN300-20031
F16568
Z104476494