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Indole-3,3'-pyrrole-2,5-dione

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Identification
Molecular formula
C18H11N3O2
CAS number
24424-99-5
IUPAC name
3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione
State
State

State at room temperature: 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione is generally found as a solid at room temperature. It remains stable under standard conditions, and its crystalline nature is preserved in dry environments. This makes it straightforward to handle in a laboratory setting, primarily when measured out in powder form.

Melting point (Celsius)
298.00
Melting point (Kelvin)
571.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
297.31g/mol
Molar mass
297.3080g/mol
Density
1.4600g/cm3
Appearence

Appearance: 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione is commonly seen as an orange-red or reddish powder. The compound tends to form crystalline structures showing clear definition and geometric edges when examined closely. It can be varied from dull to more glistening surfaces depending on purity and particle size.

Comment on solubility

Solubility of 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione

The solubility of 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione (C18H11N3O2) can be intriguing to explore due to its unique molecular structure. Understanding the solubility properties is essential for various applications, particularly in medicinal chemistry and materials science.

Solubility Characteristics

In terms of solubility:

  • Polar Solvents: This compound is expected to have limited solubility in polar solvents like water due to its hydrophobic indole rings.
  • Non-Polar Solvents: It is likely to be more soluble in non-polar organic solvents such as chloroform, dichloromethane, or ether, which can accommodate the hydrophobic regions better.
  • pH Influence: Its solubility may also change with pH alterations because of potential ionization of the nitrogen atoms in different environments.

As is often observed, the solubility behavior of complex organic compounds like 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione can be greatly influenced by structural factors and the presence of functional groups that dictate interactions with solvents.

In summary, while practical solubility data may be limited, understanding the solubility of this compound requires consideration of both its chemical structure and environmental conditions. From its expected behavior in various solvent systems, chemists can make informed decisions on how to effectively utilize this compound in practical applications.

Interesting facts

Interesting Facts about 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione

3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione, commonly referred to as a bis-indole derivative, showcases some fascinating characteristics deserving of deeper exploration:

  • Biological Relevance: This compound belongs to a class of molecules known for their biological activity. Indole-based compounds are often found in nature and have been associated with various medicinal properties, including antimicrobial and anticancer activities.
  • Chemical Structure: The unique structure features two indole moieties linked to a pyrrole-2,5-dione core. This configuration is important for its electronic properties, which can influence the reactivity and interactions of the compound.
  • Potential Applications: Researchers are examining similar compounds for applications in pharmaceuticals and organic electronics, highlighting the diverse potential of indole derivatives in modern science.
  • Synthetic Pathways: The synthesis of this compound typically involves multi-step organic reactions, allowing chemists to explore methods of creating new materials with desired functionalities. It emphasizes the creativity and skill involved in chemical synthesis.
  • Electrochemical Properties: Compounds like 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione may possess interesting electrochemical properties, making them of interest in the study of conductive polymers and electrochemical sensors.

In summary, the study of 3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione opens doors to understanding not just its role in biological systems, but also its potential technological applications. As Albert Einstein famously said, “The important thing is not to stop questioning. Curiosity has its own reason for existing.” Exploring these intriguing compounds fosters scientific curiosity and innovation.

Synonyms
bisindolylmaleimide iv
119139-23-0
3,4-di(1H-indol-3-yl)-1H-pyrrole-2,5-dione
Arcyriarubin A
Bisindolylmaleimide
3,4-Bis(3-indolyl)maleimide
3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 3,4-di-1H-indol-3-yl-
3,4-Di-1H-indol-3-yl-1H-pyrrole-2,5-dione
MFCD00236432
BIM IV
C20H13N3O2
MBK3OO5K8T
CHEMBL266487
3,4-bis(3-indolyl)-1H-pyrrole-2,5-dione
3,4-bis(1H-indol-3-yl)-2,5-dihydro-1H-pyrrole-2,5-dione
3,4-Bis(3-indolyl)maleimide (Arcyriarubin A)
Ro 31-6233
Ro-31-6233
UNII-MBK3OO5K8T
Hedysarimcoumestan E
Bisindolyl deriv. 3
Bisindolylmaleimide IV?
RO-316233
BISINDOLYMALEIMIDE IV
BIM-4
Bisindolylmaleimide deriv. 5
SCHEMBL624896
bis-indolylmaleimide deriv. 8a
BDBM2583
GTPL5937
CHEBI:92857
DTXSID30152324
GLXC-15312
HMS3229C03
HMS3401J13
HMS3648K22
BIM 4; 8; bisindolylmaleimide IV
HB0137
HSCI1_000388
NSC767269
AKOS015920110
CCG-206739
DS-0027
NSC-767269
SDCCGRCH-0000144.P001
SDCCGSBI-0086663.P004
NCGC00262009-03
DB-001961
HY-108254
B6068
CS-0027784
S0754
3,4-bis(3-indolyl)-1h-pyr-role-2,5-dione
3,4-bis-(3-indolyl)-1H-pyrrole-2,5-dione
3,4-Di-(1H-indol-3-yl)pyrrole-2,5-dione
Bisindolylmaleimide IV - CAS 119139-23-0
Bisindolylmaleimide IV, >=98% (TLC), solid
K00203
SR-01000946386
SR-01000946386-1
BRD-K49448285-001-01-3
Q27075304