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4-(9H-carbazol-3-ylamino)phenol

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Identification
Molecular formula
C18H14N2O
CAS number
658541-75-6
IUPAC name
4-(9H-carbazol-3-ylamino)phenol
State
State

At room temperature, the compound is in a solid state, with a stable crystalline form.

Melting point (Celsius)
216.50
Melting point (Kelvin)
489.65
Boiling point (Celsius)
542.30
Boiling point (Kelvin)
815.45
General information
Molecular weight
286.32g/mol
Molar mass
286.3220g/mol
Density
1.3450g/cm3
Appearence

The compound is typically a solid with a crystalline appearance. Depending on its purity, it may appear as a white to off-white powder.

Comment on solubility

Solubility of 4-(9H-Carbazol-3-ylamino)phenol

The solubility of 4-(9H-carbazol-3-ylamino)phenol can be characterized by a few key factors that influence its behavior in various solvents:

  • Polarity: The presence of both a carbazole moiety and a phenolic group suggests that this compound may exhibit moderate polarity, impacting its solubility in different environments.
  • Solvent Compatibility: This compound is likely to be soluble in polar solvents such as ethanol and methanol due to the phenolic -OH group but may show lower solubility in non-polar solvents like hexane.
  • Hydrogen Bonding: The capability of forming hydrogen bonds with solvents may enhance its solubility, making it more amenable to dissolution in aqueous solutions.
  • Temperature Dependency: As with many organic compounds, increased temperature may facilitate greater solubility, allowing for enhanced interactions between molecules.

Overall, while it can be anticipated that 4-(9H-carbazol-3-ylamino)phenol will display preferential solubility in polar solvents, precise solubility data would be essential for practical applications. As the saying goes, "solubility is a balance of forces," emphasizing the importance of understanding molecular interactions in determining solubility characteristics.

Interesting facts

Interesting Facts About 4-(9H-carbazol-3-ylamino)phenol

4-(9H-carbazol-3-ylamino)phenol, a fascinating compound in the realm of organic chemistry, boasts a unique structure that blends the properties of both carbazole and phenol. This intriguing molecule showcases an array of significant features:

  • Biological Activity: Compounds similar to 4-(9H-carbazol-3-ylamino)phenol have been studied for their potential biological activities. Some derivatives exhibit anti-cancer properties, making them of interest in pharmaceutical research.
  • Photophysical Properties: The presence of the carbazole moiety contributes to unique photophysical properties. This can result in interesting applications in organic electronics, such as light-emitting diodes (LEDs) and as a host material for phosphorescent and fluorescent dyes.
  • Versatility in Synthesis: The synthesis of this compound often involves multi-step reactions, showcasing the versatility of organic synthetic methods. This variability can lead to a diverse range of derivatives that may possess unique properties.
  • Importance in Materials Science: Compounds like 4-(9H-carbazol-3-ylamino)phenol are studied in materials science for their role in developing functional materials. Their ability to interact with light and their electrical properties make them suitable candidates for a wide array of applications.
  • Potential in Dye Chemistry: Its structural characteristics allow it to be explored as a dye or pigment. Chemists are keen to understand how modifications to this structure can enhance color properties and stability in various environments.

In summary, 4-(9H-carbazol-3-ylamino)phenol is not just a simple compound; it embodies the intersection of chemistry, biology, and materials science. As research continues to uncover new applications and functionalities, this compound serves as a reminder of the complexity and beauty found in molecular design.

Synonyms
4-(9H-Carbazol-3-ylamino)phenol
86-72-6
Phenol, 4-(9H-carbazol-3-ylamino)-
Hidrotin Blue R
Hydron Blue 3RN
Hidrotin Blue 2R
Hidrotin Blue 3R
4-(3-Carbazolylamino)phenol
r-Base
C.I. Vat Blue 47
R-Base [Czech]
Phenol, 4-(3-carbazolylamino)-
Carbazole, 3-(p-hydroxyanilino)-
3-(4'-Hydroxyfenyl)aminokarbazol
EINECS 201-693-4
NSC 75903
BRN 0247481
3-(4'-Hydroxyfenyl)aminokarbazol [Czech]
DTXSID9058947
Phenol, p-(carbazol-3-ylamino)-
4-22-00-04937 (Beilstein Handbook Reference)
NSC-75903
4-(9H-carbazol-3-yl-amino)phenol
CDU7Q26X7S
SCHEMBL7783739
DTXCID4048513
STRAHSCTRLRZNU-UHFFFAOYSA-N
HY-D0291
NSC75903
WLN: T B656 HMJ DMR DQ
3-(4'-hydroxyphenylamino)-carbazole
CS-0010203
NS00021378
Phenol, p-(carbazol-3-ylamino)-(6CI,7CI,8CI)
201-693-4