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3,3-bis(4-aminophenyl)butan-2-one

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Identification
Molecular formula
C16H18N2O
CAS number
54731-05-6
IUPAC name
3,3-bis(4-aminophenyl)butan-2-one
State
State

At room temperature, 3,3-bis(4-aminophenyl)butan-2-one is in a solid state, appearing typically as a white powder.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
268.33g/mol
Molar mass
268.3540g/mol
Density
1.1920g/cm3
Appearence

The compound 3,3-bis(4-aminophenyl)butan-2-one appears as a white crystalline powder. It is typically homogeneous in texture and color.

Comment on solubility

Solubility of 3,3-bis(4-aminophenyl)butan-2-one

The solubility of 3,3-bis(4-aminophenyl)butan-2-one can be quite intriguing due to its structural characteristics. Its solubility is influenced by several factors that are common to many organic compounds:

  • Polarity: The presence of amino groups (–NH2) in its structure contributes to polar characteristics, which can enhance solubility in polar solvents like water and alcohols.
  • Solvent Interactions: This compound may show greater solubility in solvents that can effectively interact with the amino groups. For example:
    • Polar solvents: Water, methanol, and ethanol may dissolve this compound to a degree.
    • Non-polar solvents: The solubility in non-polar solvents like hexane could be significantly lower due to incompatibility.
  • Temperature Effects: Higher temperatures often increase solubility, allowing more of the compound to dissolve in a given volume of solvent.

In conclusion, while 3,3-bis(4-aminophenyl)butan-2-one shows preferential solubility in polar solvents, its actual solubility can vary widely based on specific conditions. As a reminder, always conduct experiments under controlled conditions to verify solubility behavior.

Interesting facts

Interesting Facts About 3,3-bis(4-aminophenyl)butan-2-one

3,3-bis(4-aminophenyl)butan-2-one, commonly known for its intriguing structure and multifaceted applications, holds a special place in organic chemistry. Here are some captivating facts about this compound:

  • Versatile Building Block: This compound serves as a versatile building block in organic synthesis, allowing chemists to create a variety of complex molecules and materials.
  • Pharmaceutical Relevance: Due to its structural similarity to various biologically active molecules, it has potential applications in drug development, particularly as intermediates in the synthesis of pharmaceuticals.
  • Research Applications: 3,3-bis(4-aminophenyl)butan-2-one is often studied in materials science for its properties that could influence the development of new polymer composites, specifically those that require enhanced thermal and mechanical properties.
  • Chemical Reactivity: The presence of amino groups in its structure contributes to its reactivity, making it a valuable compound for creating derivatives that may exhibit unique traits, such as improved solubility or bioactivity.
  • Stimulating Scientific Inquiry: The compound has been a topic of inquiry in various chemical studies, leading to fascinating findings that broaden our understanding of structure-activity relationships within organic compounds.

As a student or an enthusiast in chemistry, it’s inspiring to explore the implications and potential applications of 3,3-bis(4-aminophenyl)butan-2-one. According to one study, "The structural characteristics of this compound provide numerous avenues for innovation in both organic synthesis and materials science."
Embracing such compounds opens up a world of creativity and discovery in the fascinating realm of chemistry!

Synonyms
Amphenone B
amphenone
3,3-bis(4-aminophenyl)butan-2-one
UNII-Y2YUN941SL
Y2YUN941SL
2-Butanone, 3,3-bis(4-aminophenyl)-
AMPHENONE B [MI]
3,3-Bis(4-aminophenyl)-2-butanone
2-Butanone, 3,3-bis(p-aminophenyl)-
DTXSID70181370
DTXCID80103861
2686-47-7
AC1L2AAH
Amphenon B
SureCN8333956
CHEBI:2678
SCHEMBL8333956
C07616
Q27105763