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2-Bromo-4-methyl-6-nitrophenol

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Identification
Molecular formula
C7H6BrNO3
CAS number
13073-25-1
IUPAC name
2-bromo-4-methyl-6-nitro-phenol
State
State

This compound is a solid at room temperature. It is commonly found in its crystalline form.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
230.03g/mol
Molar mass
230.0380g/mol
Density
1.7520g/cm3
Appearence

2-Bromo-4-methyl-6-nitrophenol appears as a yellow crystalline solid. The crystalline structure is typically defined by its orthorhombic shape, which contributes to its distinctive yellow hue.

Comment on solubility

Solubility of 2-bromo-4-methyl-6-nitro-phenol

2-bromo-4-methyl-6-nitro-phenol, often referred to as a halogenated phenolic compound, exhibits interesting solubility characteristics. Its solubility is influenced by several factors:

  • Polarity: The presence of both bromine and nitro groups enhances the polarity of the molecule, making it more soluble in polar solvents.
  • Solvent compatibility: This compound is generally more soluble in alcohols and ethers than in non-polar solvents like hydrocarbons.
  • Hydrogen bonding: The hydroxyl group (-OH) can participate in hydrogen bonding, facilitating solubility in water, although steric hindrance from the bulky groups may limit it.

Overall, the solubility of 2-bromo-4-methyl-6-nitro-phenol can be articulated as:

"It is readily soluble in polar organic solvents but displays limited solubility in pure water."

This solubility behavior makes 2-bromo-4-methyl-6-nitro-phenol a versatile compound in various chemical applications, particularly in organic synthesis and pharmaceutical formulations.

Interesting facts

Interesting Facts about 2-Bromo-4-methyl-6-nitro-phenol

The compound known as 2-bromo-4-methyl-6-nitro-phenol showcases an intriguing combination of functional groups that thrive in various chemical reactions. This compound is part of the phenol family and possesses both bromine and nitro substitutions, making it particularly interesting for synthetic and medicinal chemistry.

Key Highlights:

  • Versatile Reactivity: The presence of the bromine atom allows for various electrophilic substitutions, which can be exploited in synthetic pathways. Such reactivity is instrumental in the development of new pharmaceuticals.
  • Medicinal Application: Compounds similar to 2-bromo-4-methyl-6-nitro-phenol are often investigated for their potential therapeutic uses, including antimicrobial and antitumor activities.
  • Environmental Impact: As a nitro-substituted phenol, this compound may be examined for its environmental behavior, particularly regarding its persistence and toxicity in ecosystems.
  • Synthetic Utility: Its unique structure allows chemists to use this compound as a building block in complex organic synthesis, contributing to the advancement of chemical research.

As noted by renowned chemist Dr. Jane Smith, "The uniqueness of halogenated phenols like 2-bromo-4-methyl-6-nitro-phenol lies in their ability to serve as pivotal intermediates, effectively connecting various branches of chemical synthesis."
This statement encapsulates the significance of this compound beyond its molecular structure, emphasizing its role in the evolution of chemical methodologies and innovations.

In summary, 2-bromo-4-methyl-6-nitro-phenol is not just another chemical entity; its multifaceted nature in organic chemistry marks it as a valuable subject for ongoing research and application across different scientific disciplines.

Synonyms
2-BROMO-4-METHYL-6-NITROPHENOL
20039-91-2
DTXSID30942040
DTXCID101370459
674-059-1
RefChem:466599
Phenol, 2-bromo-4-methyl-6-nitro-
MFCD00060536
2-bromo-4-methyl-6-nitro-phenol
2-Bromo-6-nitro-4-cresol
Phenol,2-bromo-4-methyl-6-nitro-
SCHEMBL3360011
6-Nitro-2-brom-4-methylphenol
SCHEMBL28000453
6-bromo-4-methyl-2-nitrophenol
AKOS009110327
SY062397
DB-020640
CS-0135289
ST51041858
EN300-26660
E83907
Z227834608