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4'-Nitroacetophenone

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Identification
Molecular formula
C14H11NO3
CAS number
134-85-0
IUPAC name
1-[4-(4-nitrophenyl)phenyl]ethanone
State
State

The compound is a solid at room temperature. Due to its crystalline nature, it can appear as either a fine powder or larger crystals depending on its preparation and handling.

Melting point (Celsius)
83.00
Melting point (Kelvin)
356.15
Boiling point (Celsius)
346.50
Boiling point (Kelvin)
619.65
General information
Molecular weight
243.24g/mol
Molar mass
181.1680g/mol
Density
1.2913g/cm3
Appearence

4'-Nitroacetophenone is typically a pale yellow to tan crystalline powder. It is known for its distinct crystalline structure that catches light, giving it a somewhat sparkly appearance. The powder may slightly darken upon prolonged exposure to air and light.

Comment on solubility

Solubility of 1-[4-(4-nitrophenyl)phenyl]ethanone

The solubility of 1-[4-(4-nitrophenyl)phenyl]ethanone, a compound with complex aromatic structures, is influenced by several key factors. Understanding these factors can provide insights into its behavior in various solvents:

  • Polarity: Given its molecular structure, which includes both electron-withdrawing nitro groups and hydrophobic phenyl rings, the overall polarity of the compound plays a crucial role in its solubility.
  • Solvent Interaction: 1-[4-(4-nitrophenyl)phenyl]ethanone is expected to exhibit better solubility in non-polar or weakly polar solvents like toluene or dichloromethane. In contrast, it may have limited solubility in highly polar solvents such as water.
  • Temperature Effects: The solubility can increase with temperature, thus heating the solvent can sometimes expedite the dissolution process.
  • Concentration and Crystallization: At certain concentrations, this compound may also tend to crystallize out of solution, particularly if the solvent is not adequately chosen based on its solubility characteristics.

In summary, while 1-[4-(4-nitrophenyl)phenyl]ethanone may exhibit limited solubility in highly polar media, its solubility profile can potentially be optimized by selecting the appropriate solvent and adjusting temperature conditions. As one source notes, "the choice of solvent is key to unlocking the solubility of complex organic compounds." Therefore, careful consideration of these factors will allow for effective handling and application of this compound in various chemical processes.

Interesting facts

Interesting Facts about 1-[4-(4-nitrophenyl)phenyl]ethanone

1-[4-(4-nitrophenyl)phenyl]ethanone is a fascinating compound with a rich background in organic chemistry. Often utilized in various chemical reactions and applications, this compound stands out due to its unique structural characteristics and the presence of nitro groups which enhance its chemical reactivity. Here are some intriguing aspects of this compound:

  • Structure and Functional Groups: The compound features a ketone functional group, known for its role in a variety of chemical transformations. The aromatic nitrophenyl groups contribute to the compound's reactivity, making it a valuable target for synthetic chemistry.
  • Importance in Research: This compound is often studied for its potential applications in pharmaceuticals and materials science, particularly in the creation of dyes and pigments due to its colored properties.
  • Reactivity: The nitro group attached to the phenyl ring can serve as a versatile handle for further chemical modifications, enabling chemists to explore a range of synthetic pathways.
  • Environmental Considerations: With the increasing interest in sustainable chemistry, compounds like 1-[4-(4-nitrophenyl)phenyl]ethanone are scrutinized for their environmental impact, especially regarding the safety of nitro compounds.

In summary, 1-[4-(4-nitrophenyl)phenyl]ethanone exemplifies the complexity and beauty of organic compounds. Its *reactive nature*, coupled with potential applications, makes it an exciting subject for both students and professionals alike. As noted by chemists, “The journey through understanding chemical compounds is a path filled with surprises and discoveries.”

Synonyms
4-Acetyl-4'-nitrobiphenyl
135-69-3
4'-(p-Nitrophenyl)acetophenone
Acetophenone, 4'-(p-nitrophenyl)-
1-[4-(4-nitrophenyl)phenyl]ethanone
Ethanone, 1-(4'-nitro[1,1'-biphenyl]-4-yl)-
EINECS 205-212-9
NSC 43063
DTXSID1059656
Ethanone, 1-(4'-nitro(1,1'-biphenyl)-4-yl)-
NSC-43063
1-(4'-Nitro[1,1'-biphenyl]-4-yl)ethanone
1-(4/'-nitro[1,1/'-biphenyl]-4-yl)ethan-1-one
NSC43063
GCC2USS8ZR
4'-nitro-4-acetylbiphenyl
SCHEMBL6703081
DTXCID4034289
1-(4'-nitrobiphenyl-4-yl)ethanone
4'-nitro-4-acetyl-1,1'-biphenyl
STK290996
AKOS003363905
1-(4'-Nitro-biphenyl-4-yl)-ethanone
Acetophenone, 4'-(p-nitrophenyl)-(8CI)
NS00024395
1-(4'-Nitro[1,1'-biphenyl]-4-yl)ethanone #
1-(4'-Nitro(1,1'-biphenyl)-4-yl)ethan-1-one