Skip to main content

5,11-Dihydroindolo[3,2-b]carbazole-12-carbaldehyde

ADVERTISEMENT
Identification
Molecular formula
C19H12N2O
CAS number
114725-76-5
IUPAC name
5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde
State
State

At room temperature, 5,11-Dihydroindolo[3,2-b]carbazole-12-carbaldehyde exists as a solid. Handling requires consideration of its stability and solubility in various solvents for applications in chemical synthesis and materials science.

Melting point (Celsius)
222.00
Melting point (Kelvin)
495.15
Boiling point (Celsius)
431.00
Boiling point (Kelvin)
704.15
General information
Molecular weight
294.31g/mol
Molar mass
294.3100g/mol
Density
1.3200g/cm3
Appearence

5,11-Dihydroindolo[3,2-b]carbazole-12-carbaldehyde typically appears as a pale yellow to off-white crystalline powder. This appearance is maintained under standard conditions and may be used to identify the compound in laboratory settings.

Comment on solubility

Solubility of 5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde (C19H12N2O)

The solubility of 5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde in various solvents is a crucial aspect of its chemical behavior and applications. Its structure suggests significant hydrophobic character, making it less likely to dissolve in water. Here's a closer look at its solubility characteristics:

  • Polar Solvents: The compound is expected to have low solubility in polar solvents, such as water, due to its non-polar indole and carbazole ring structures. The presence of a carbonyl group might provide some interaction potential, but overall solubility remains limited.
  • Non-Polar Solvents: It shows a higher tendency to dissolve in non-polar solvents, like toluene or chloroform, owing to Van der Waals interactions and the hydrophobic nature of its aromatic rings.
  • Practical Implications: This solubility behavior is essential for applications involving organic synthesis and materials, where a suitable solvent can enhance reaction efficiencies and product yields.

In summary, while 5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde exhibits limited solubility in polar solvents, it benefits from enhanced solubility in various organic solvents. Understanding its solubility profile is vital for effective chemical handling and maximizing its utility in research and industry.

Interesting facts

Interesting Facts about 5,11-Dihydroindolo[3,2-b]carbazole-12-carbaldehyde

5,11-Dihydroindolo[3,2-b]carbazole-12-carbaldehyde is a fascinating compound with unique structural features and intriguing implications in various fields of research. Here are some interesting facts about this compound:

  • Structure: The structure of this compound involves a complex arrangement of an indole and carbazole system, indicating that it belongs to the family of polycyclic aromatic hydrocarbons. This complex aromatic structure contributes to its unique chemical properties.
  • Biological Activity: Research has shown that derivatives of indolo[3,2-b]carbazole possess significant biological activity, including *antitumor* and *antimicrobial* properties. The presence of the aldehyde group in the compound adds to its reactivity, allowing it to participate in various chemical reactions that can enhance its medicinal potential.
  • Synthetic Routes: The synthesis of this compound can involve several methods, including multi-step organic reactions. *Chemists often explore different routes to optimize yield and purity,* showcasing the importance of innovation in organic synthesis.
  • Potential Applications: Due to its interesting properties, 5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde could play a role in the development of novel pharmaceuticals and materials. Its incorporation into larger frameworks could lead to new discoveries in fields such as *organic electronics* or *photovoltaics*.
  • Research Interest: The compound represents an area of active research as scientists seek to better understand its properties and explore its potential as a scaffold for drug discovery. *Exploring the structure-activity relationship is crucial* in this context and could lead to exciting new findings.

In summary, 5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde is not just a compound of interest for its structure, but also for its potential implications in pharmaceuticals and materials science. As research continues, it presents numerous opportunities for discovery and innovation.

Synonyms
FICZ
172922-91-7
6-formylindolo[3,2-b]carbazole
5,11-dihydroindolo[3,2-b]carbazole-6-carbaldehyde
229020-82-0
5,11-dihydroindolo[3,2-b]carbazole-12-carbaldehyde
6-formylindolo(3,2-b)carbazole
Indolo[3,2-b]carbazole-6-carboxaldehyde, 5,11-dihydro-
CHEMBL472031
DTXSID30274338
6-FORMYLINDOLO [3,2-B] CARBAZOLE
5,11-Dihydroindolo(3,2-b)carbazole-6-carbaldehyde
FICZ-carbazole
5,11-dihydroindolo(3,2-b)carbazole-12-carbaldehyde
5H,11H-indolo[3,2-b]carbazole-6-carbaldehyde
Bio1_000123
MFCD09879259
A1LWI
Spectrum5_001953
CBiol_001837
BSPBio_001455
KBioGR_000175
KBioSS_000175
SCHEMBL528520
5,11-Dihydroindolo[3,2-b]carbazole-6-carboxaldehyde
BML3-F10
CHEBI:94466
KBio2_000175
KBio2_002743
KBio2_005311
KBio3_000349
KBio3_000350
DTXCID60225818
Bio1_000612
Bio1_001101
Bio2_000175
Bio2_000655
HMS1361I17
HMS1791I17
HMS1989I17
HMS3402I17
BCP26067
BDBM50541262
s9682
AKOS016344677
CS-3513
IDI1_033925
NCGC00161390-01
NCGC00161390-02
NCGC00161390-03
NCGC00161390-04
NCGC00161390-05
DA-63441
DS-15051
HY-12451
C73318
5,11-dihydroindolo[3,2-b]carbazole-12-carboxaldehyde
BRD-K00184207-001-02-4
Q27166328
683-412-9