Skip to main content

4-amino-3-methylbenzophenone

ADVERTISEMENT
Identification
Molecular formula
C14H13NO
CAS number
24238-61-1
IUPAC name
(4-amino-3-methyl-phenyl)-phenyl-methanone
State
State

At room temperature, 4-amino-3-methylbenzophenone exists as a solid. It remains stable in this form under standard conditions of temperature and pressure.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
211.27g/mol
Molar mass
211.2660g/mol
Density
1.1450g/cm3
Appearence

4-Amino-3-methylbenzophenone typically appears as a yellow to brown crystalline solid. Its crystalline form can range from fine powder to larger granules, depending on the specific preparation and handling processes used.

Comment on solubility

Solubility of (4-amino-3-methyl-phenyl)-phenyl-methanone

(4-amino-3-methyl-phenyl)-phenyl-methanone, also known by its IUPAC name, exhibits interesting solubility characteristics that are essential for its applications and behavior in various environments.

General Solubility Properties

This compound's solubility can be influenced by several factors:

  • Polar vs. Non-polar Solvents: Due to the presence of an amino group and the overall molecular framework, (4-amino-3-methyl-phenyl)-phenyl-methanone is expected to have better solubility in polar solvents compared to non-polar solvents.
  • Hydrogen Bonding: The amino group can form hydrogen bonds, which can enhance solubility in water and other polar solvents.
  • Molecular Size: The larger size of the molecule compared to simple amines can restrict solubility in certain solvents.

Specific Solubility Characteristics

While detailed solubility data may not be extensively documented, it is often observed that:

  • Compounds containing amino groups tend to be more soluble in water.
  • Microscopic analysis may reveal that solubility varies with temperature, as warmer conditions typically increase solubility.
  • The presence of substituents like methyl groups can influence the hydrophobic interactions, thereby affecting solubility levels.

It is crucial to consider these factors when evaluating (4-amino-3-methyl-phenyl)-phenyl-methanone's potential uses. In practical applications, the solubility can significantly affect the compound's reactivity and availability in biological systems, making understanding its solubility a key aspect of research and development.

Interesting facts

Interesting Facts about (4-amino-3-methyl-phenyl)-phenyl-methanone

(4-amino-3-methyl-phenyl)-phenyl-methanone, also known as a type of ketone, is a fascinating compound with a variety of applications and characteristics that make it noteworthy in the field of chemistry. Here are some interesting aspects of this compound:

  • Pharmaceutical Relevance: This compound is structurally similar to various drug molecules, and its unique functional groups can influence biological activity, making it a subject of interest in drug design and discovery.
  • Versatile Applications: Due to its functional characteristics, it is used in synthetic chemistry to produce a variety of organic compounds, showcasing its importance in material science and organic synthesis.
  • Structural Significance: The combination of an amino group and a ketone structure suggests potential for engaging in hydrogen bonding, which can affect solubility and reactivity patterns with other compounds.
  • Synthesis Insights: The synthesis of this compound often involves intricate organic reactions, including the Friedel-Crafts acylation or coupling reactions, which are vital techniques in expanding molecular diversity in organic chemistry.
  • Derivative Exploration: Researchers are keen on exploring derivatives of this compound as they may exhibit enhanced properties or novel applications, leading to ongoing studies in medicinal chemistry and materials science.

To quote a prominent chemist: "The beauty of organic chemistry lies in the transformation of simple structures into complex and functional entities." This statement resonates particularly well with compounds like (4-amino-3-methyl-phenyl)-phenyl-methanone, as it embodies the essence of chemical creativity and exploration.

In summary, (4-amino-3-methyl-phenyl)-phenyl-methanone serves as a vibrant example of the intricacies of organic chemistry, compelling scientists and students alike to appreciate the depth and potential of chemical compounds.

Synonyms
4-Amino-3-methylbenzophenone
4934-55-8
3-Methyl-4-aminobenzophenone
BENZOPHENONE, 4-AMINO-3-METHYL-
3-Metil-4-ammino-benzofenone
BRN 2100422
3-Metil-4-ammino-benzofenone [Italian]
Methanone, (4-amino-3-methylphenyl)phenyl-
DTXSID10197773
3-14-00-00245 (Beilstein Handbook Reference)
DTXCID70120264
SCHEMBL4609604
ZCVUMNJAVAXADT-UHFFFAOYSA-N
AKOS013511822
(4-Amino-3-methylphenyl)(phenyl)methanone
DB-131016