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2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol

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Identification
Molecular formula
C14H21BrO2
CAS number
78478-82-7
IUPAC name
2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol
State
State

At room temperature, this compound is typically a crystalline solid. Depending on conditions such as humidity and light exposure, its appearance may vary.

Melting point (Celsius)
58.00
Melting point (Kelvin)
331.15
Boiling point (Celsius)
412.20
Boiling point (Kelvin)
685.35
General information
Molecular weight
289.22g/mol
Molar mass
289.2090g/mol
Density
1.3540g/cm3
Appearence

The compound typically appears as a crystalline solid. The precise nature and color can vary depending on purity and specific conditions of crystallization.

Comment on solubility

Solubility of 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol

The solubility of 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol can be assessed based on its molecular structure and functional groups. This compound contains both hydrophobic and hydrophilic elements, which can affect its solubility in various solvents.

Factors Influencing Solubility

  • Hydrophobic Character: The long alkane chain and bromophenyl group contribute to its hydrophobic nature, which may limit solubility in polar solvents.
  • Hydrophilic Groups: The presence of hydroxyl groups (-OH) in the structure enhances its potential solubility in polar solvents like water.
  • Temperature: Generally, solubility increases with temperature, and thus may vary significantly under different conditions.

As a result, 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol is likely to exhibit moderate solubility in polar organic solvents and lower solubility in nonpolar solvents. The balance between its hydrophobic and hydrophilic components plays a crucial role in determining its overall solubility profile.

In conclusion, while there may be some degree of solubility in aqueous solutions due to the -OH groups, the significant hydrophobic portions suggest that perfect solubility in water may be limited.

Interesting facts

Interesting Facts about 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol

This fascinating compound, 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol, belongs to a class of organic compounds known for their diverse biological activities. Let's delve into some intriguing insights about this compound:

  • Structure and Functionality: The presence of a bromophenyl group and a hydroxy functional group gives this compound unique properties, making it suitable for various applications in pharmaceuticals and organic synthesis.
  • Biological Importance: Compounds like this one are often investigated for their potential as pharmacologically active agents. Research may focus on their role in inhibiting specific biological pathways or acting as intermediates during the synthesis of more complex drugs.
  • Synthetic Versatility: The two alcohol (diol) substituents in the structure enhance its ability to participate in further chemical reactions, allowing chemists to create a variety of derivatives that can be tailored for specific applications.
  • Potential for Reactivity: With typical reactivities associated with bromides, 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol can act as a nucleophile in various substitution reactions. This feature is particularly valuable in synthetic organic chemistry.
  • Research Applications: This compound’s structure opens doors for research in fields such as medicinal chemistry, biochemistry, and material science, due to its potential interactions and modifications.

In summary, the study of 2-(4-bromophenyl)-4-ethyl-hexane-2,4-diol exemplifies the intricate relationship between a compound's structure and its potential applications. As researchers continue to explore the characteristics and utility of compounds like this, we may see exciting advancements in the fields of pharmaceuticals and organic synthesis.

Synonyms
2-(4-bromophenyl)-4-ethylhexane-2,4-diol
21133-89-1
DTXSID20943460
2,4-HEXANEDIOL, 2-(p-BROMOPHENYL)-4-ETHYL-
RD 6013
BRN 2115773
RefChem:1061177
p-Bromophenyl-1-methyl-1-diethyl-3,3 propanediol-1,3
DTXCID001371828