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
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:
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.