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1,3-dimethyl-5-(4-nitrophenoxy)benzene

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Identification
Molecular formula
C14H13NO3
CAS number
124781-99-9
IUPAC name
1,3-dimethyl-5-(4-nitrophenoxy)benzene
State
State

At room temperature, 1,3-dimethyl-5-(4-nitrophenoxy)benzene is typically a solid.

Melting point (Celsius)
90.50
Melting point (Kelvin)
363.70
Boiling point (Celsius)
350.50
Boiling point (Kelvin)
623.70
General information
Molecular weight
241.26g/mol
Molar mass
241.2690g/mol
Density
1.2100g/cm3
Appearence

This compound typically appears as a yellow crystalline solid.

Comment on solubility

Solubility of 1,3-Dimethyl-5-(4-nitrophenoxy)benzene

1,3-Dimethyl-5-(4-nitrophenoxy)benzene exhibits notable solubility characteristics that are influenced by its molecular structure. This compound, a substituted aromatic hydrocarbon, has specific solubility tendencies in various solvents:

  • Polar solvents: The presence of the (4-nitrophenoxy) group can interact favorably with polar solvents due to potential dipole interactions. As a result, it may show some degree of solubility in polar organic solvents such as ethanol and acetone.
  • Nonpolar solvents: Given its aromatic nature and hydrophobic (1,3-dimethyl) groups, it is more likely to be soluble in nonpolar solvents like toluene or hexane, aligning with the principle of "like dissolves like."

However, it is essential to note that the overall solubility will depend on factors such as temperature and the presence of other solutes. As with many aromatic compounds, crystallization may occur when transitioning from solution to solid state, particularly if the solvent is not suitably chosen.

In summary, while 1,3-dimethyl-5-(4-nitrophenoxy)benzene is anticipated to be soluble in a range of organic solvents, specific interactions and solvation phenomena play crucial roles in its solubility profile. Experimentation is recommended to determine precise solubility limits.

Interesting facts

Interesting Facts about 1,3-Dimethyl-5-(4-nitrophenoxy)benzene

1,3-Dimethyl-5-(4-nitrophenoxy)benzene is a fascinating compound that showcases the versatility and complexity of organic chemistry. Here are some intriguing aspects of this compound:

  • Substituent Variety: The molecule features multiple substituents, including dimethyl and 4-nitrophenoxy groups, each contributing uniquely to the chemical properties of the compound. It's a perfect example of how alterations in structure can lead to different reactivity and functionalities.
  • Applications in Industry: Compounds like this one are often used as intermediates in the synthesis of more complex organic molecules. They play a crucial role in the production of dyes, pesticides, and pharmaceuticals, highlighting their importance in applied chemistry.
  • Research Potential: The nitrophenyl group is well-known for its role in various reactions, including nucleophilic substitutions. This makes 1,3-dimethyl-5-(4-nitrophenoxy)benzene a potential candidate for research in synthetic organic chemistry and materials science.
  • Structure-Activity Relationship (SAR): Understanding how variations in groups attached to the benzene ring affect biological activity is crucial in medicinal chemistry. This compound provides an excellent platform for studying SAR, which can lead to the development of new therapeutic agents.

In the words of a famous chemist, "Chemistry, in its essence, is all about the relationships between molecules." This compound embodies that sentiment, serving as a bridge between basic science and practical applications. Whether for academic research or industrial use, its distinctive structure and properties continue to intrigue chemists around the world.

Synonyms
1,3-Dimethyl-5-(4-nitrophenoxy)benzene
1630-17-7
Benzene, 1,3-dimethyl-5-(4-nitrophenoxy)-
DTXSID5075103
DTXCID6035237
DMNP
5-(4-nitrophenoxy) m-xylene
SCHEMBL1323759
ALBB-034772
AKOS021982745
HS-6291
3,5-dimethylphenyl 4-nitrophenyl ether