N-(4-phenylphenyl)acetamide | Solubility of Things

Identification

Molecular formula

C₁₄H₁₃NO

CAS number

3607-18-7

IUPAC name

N-(4-phenylphenyl)acetamide

State

At room temperature, N-(4-phenylphenyl)acetamide is a solid. It is commonly used in scientific research and its state as a solid is typical for organic compounds of its molecular size and composition.

Melting point (Celsius)

163.00

Melting point (Kelvin)

436.15

Boiling point (Celsius)

279.00

Boiling point (Kelvin)

552.15

General information

Molecular weight

211.27g/mol

Molar mass

211.2680g/mol

Density

1.1900g/cm³

Appearence

N-(4-phenylphenyl)acetamide is typically found as an off-white to light yellow crystalline solid. It may appear as powder or crystals and is usually characterized by its aromatic structure, contributing to its unique appearance when evaluated in pure form.

Comment on solubility

Solubility of N-(4-phenylphenyl)acetamide

N-(4-phenylphenyl)acetamide, with the chemical formula C₁₅H₁₅NO, exhibits interesting solubility properties that are worth exploring. Understanding the solubility of this compound can provide insight into its potential applications and behavior in various environments.

Typically, the solubility of amides in solvents is influenced by several factors, including:

Molecular Structure: The presence of both hydrophobic phenyl groups and a hydrophilic acetamide functional group affects solubility.
Polarity: Amides generally possess moderate polarity, which can enhance their solubility in polar solvents like water and alcohols.
Temperature: Increased temperature often increases solubility, allowing compounds to dissolve more readily in their respective solvents.

For N-(4-phenylphenyl)acetamide, it is usually observed that:

It shows some solubility in organic solvents such as ethanol and acetone.
Its solubility in water is limited due to the large hydrophobic phenyl groups which tend to aggregate and hinder dissolution.

In conclusion, while N-(4-phenylphenyl)acetamide may dissolve adequately in certain organic solvents, it exhibits limited solubility in water. This characteristic can have profound implications for its use in various chemical processes and formulations.

Interesting facts

Exploring N-(4-phenylphenyl)acetamide

N-(4-phenylphenyl)acetamide, a fascinating organic compound, belongs to the class of amides. This compound is particularly interesting due to its structural features and potential applications in various fields.

Key Features

Structure: The compound consists of an acetamide functional group attached to a phenyl ring that is further substituted by another phenyl group. This unique arrangement allows for interesting interactions between different molecular elements.
Properties: Due to its structure, this compound can exhibit properties such as selective binding and responsiveness to changes in the environment, making it a candidate for research in materials science and chemistry.
Potential Applications: There is a growing interest in exploring the use of N-(4-phenylphenyl)acetamide as a precursor for drugs, agrochemicals, and in organic synthesis, highlighting its versatility.

Research Significance

Interestingly, studies on N-(4-phenylphenyl)acetamide have suggested its potential role in:

Pharmaceuticals: It may play a role in the development of medications due to its molecular characteristics.
Polymer Science: Its distinctive structure offers possibilities for incorporation into polymers, enhancing their properties.
Biological Studies: Its interaction with biological molecules can yield insights into molecular recognition processes.

Conclusion

In summary, N-(4-phenylphenyl)acetamide is more than just a chemical compound; it is a gateway to a world of scientific exploration. As researchers continue to delve deeper into its properties and applications, this compound may prove essential in advancing multiple disciplines.

Synonyms

4-ACETYLAMINOBIPHENYL

N-Acetyl-4-aminobiphenyl

N-(4-phenylphenyl)acetamide

p-Phenylacetanilide

4-Biphenylacetamide

N-4-Biphenylacetamide

Biphenyl, 4-acetamido

CCRIS 734

(4-Biphenyl)acetamide

Acetamide, N-[1,1'-biphenyl]-4-yl-

HSDB 5068

N-(4-Biphenyl)acetamide

UNII-U9BHQ2TJ87

N-(1,1'-Biphenyl)-4-ylacetamide

U9BHQ2TJ87

BRN 2097736

Acetamide, N-(1,1'-biphenyl)-4-yl-

AI3-01431

NSC-3134

N-(1,1'-Biphenyl-4-yl)acetamide

NSC-65931

NSC-227192

ACETYLAMINOBIPHENYL, 4-

DTXSID8039243

4-12-00-03248 (Beilstein Handbook Reference)

4-ACETYLAMINOBIPHENYL [HSDB]

NAcetylxenylamin

pPhenylacetanilide

4Acetamidobiphenyl

4Biphenylacetamide

4'Fenylacetanilid

N4Biphenylacetamide

4'Phenylacetanilide

4Biphenylacetylamide

Acetanilide, pphenyl

NAcetyl4aminobiphenyl

Biphenyl, 4acetamido

NAcetoxy4aminobiphenyl

Acetanilide, 4'phenyl

N(4Biphenylyl)acetamide

DTXCID3016

N(1,1'Biphenyl)4ylacetamide

Acetamide, N(1,1'biphenyl)4yl

817-898-2

svldilrdqovjed-uhfffaoysa-n

4075-79-0

N-([1,1'-Biphenyl]-4-yl)acetamide

4'-Phenylacetanilide

4-Acetamidobiphenyl

4-Biphenylacetylamide

Acetanilide, p-phenyl-

Acetanilide, 4'-phenyl-

N-(4-Biphenylyl)acetamide

N-Acetylxenylamin

4-(Acetylamino)biphenyl

4'-Fenylacetanilid

N-Biphenyl-4-yl-acetamide

NSC 3134

NSC 65931

4-Phenylacetanilide

NSC 227192

N-{[1,1'-biphenyl]-4-yl}acetamide

WLN: 1VMR DR

Acetamide,1'-biphenyl]-4-yl-

N-Acetylxenylamin [Czech]

4'-Fenylacetanilid [Czech]

N-biphenyl-4-ylacetamide

4-acetaminobiphenyl

Maybridge3_005462

ACETAMIDE,N-[1,1'-BIPHENYL]-4-YL-

4-acetamido-1,1'biphenyl

N-(biphenyl-4-yl)acetamide

NCIOpen2_002951

4-acetamido-1,1'-biphenyl

SCHEMBL171741

CHEMBL300429

NSC3134

CHEBI:177487

HMS1446I06

NSC65931

MFCD00276655

NSC227192

STK396441

AKOS000121530

HS-3095

N-[1,1'-Biphenyl]-4-ylacetamide #

IDI1_016849

DB-340009

NS00017496

EN300-15554

C20285

Q27290959

Z30177125