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N-(3-phenylphenyl)acetamide

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Identification
Molecular formula
C14H13NO
CAS number
2433-71-0
IUPAC name
N-(3-phenylphenyl)acetamide
State
State
This compound is typically a solid at room temperature. It is generally stable and not volatile in nature.
Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
372.00
Boiling point (Kelvin)
645.15
General information
Molecular weight
211.26g/mol
Molar mass
211.2610g/mol
Density
1.0499g/cm3
Appearence

This compound appears as a white to off-white crystalline solid. The appearance may vary slightly based on purity and form (e.g., crystalline or powder).

Comment on solubility

Solubility of N-(3-phenylphenyl)acetamide

N-(3-phenylphenyl)acetamide, often referred to for its unique structure, exhibits interesting solubility characteristics in various solvents. Its solubility can be influenced significantly by factors such as temperature, solvent type, and molecular interactions.

Key Points Regarding Solubility:

  • Polarity of Solvents: N-(3-phenylphenyl)acetamide is generally more soluble in polar organic solvents like ethanol, methanol, and acetone compared to non-polar solvents.
  • Temperature Dependence: Solubility tends to increase with temperature, making it more soluble at higher temperatures.
  • Chemical Interactions: Hydrogen bonding and van der Waals forces can play significant roles in the solubility profile of this compound.
  • Concentration Factors: At high concentrations, the solubility may be limited due to potential aggregation or crystallization effects.

In summary, while N-(3-phenylphenyl)acetamide demonstrates moderate solubility in polar solvents, its overall solubility profile is complex and depends on various chemical and physical factors. Understanding these relationships is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about N-(3-phenylphenyl)acetamide

N-(3-phenylphenyl)acetamide, a fascinating organic compound, belongs to the class of amides and plays a significant role in various fields of chemistry and biochemistry. Here are some intriguing aspects of this compound:

  • Derivative of Acetamide: This compound is a derivative of acetamide, highlighting the significance of functional groups in organic chemistry. The presence of phenyl groups adds aromatic characteristics that can influence its reactivity and interaction.
  • Potential Pharmaceutical Applications: Compounds like N-(3-phenylphenyl)acetamide have been researched for their potential medicinal properties. They may exhibit biological activity, making them candidates for drug development in treating various ailments.
  • Research Interest: The structural arrangement of N-(3-phenylphenyl)acetamide has garnered attention in scientific literature. Researchers are often fascinated by how its unique structure can lead to different physical and chemical properties compared to similar compounds.
  • Importance of Aromaticity: The two phenyl groups in the compound contribute to its aromatic nature. This could potentially affect its interactions with other molecules, including enzymes or receptors in biological systems.
  • Intermolecular Interactions: The packing and arrangement of these molecules can lead to interesting intermolecular forces, which may impact the compound's behavior in different environments, such as in solution or in solid form.

In summary, N-(3-phenylphenyl)acetamide is an exemplary compound that bridges fundamental organic chemistry with potential real-world applications, especially in pharmaceuticals and materials science. Its intriguing structure and properties make it an interesting subject of study for chemists and researchers alike.

Synonyms
3-Acetamidobiphenyl
3'-Phenylacetanilide
N-Acetoxy-3-aminobiphenyl
3-Acetylaminobiphenyl
N-(3-Biphenylyl)acetamide
ACETANILIDE, 3'-PHENYL-
N-(1,1'-Biphenyl)-3-ylacetamide
BRN 2097490
Acetamide, N-(1,1'-biphenyl)-3-yl-
DTXSID40175362
N-[1,1'-biphenyl]-3-ylacetamide
4-12-00-03239 (Beilstein Handbook Reference)
Acetamide, N-[1,1'-biphenyl]-3-yl-
DTXCID2097853
Acetamide, N-(1,1'-biphenyl)-3-yl-(9CI)
2113-54-4
SCHEMBL3786463