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Bis(indolyl)methane

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Identification
Molecular formula
C17H14N2
CAS number
6892-68-8
IUPAC name
1-(1H-indol-3-yl)-N-(1H-indol-3-ylmethyleneamino)methanimine
State
State

At room temperature, bis(indolyl)methane is in a solid state, typically a crystalline powder.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
481.00
Boiling point (Kelvin)
754.15
General information
Molecular weight
286.33g/mol
Molar mass
286.3330g/mol
Density
1.4500g/cm3
Appearence

Bis(indolyl)methane typically appears as a solid, usually in the form of a pale yellow or off-white powder.

Comment on solubility

Solubility of 1-(1H-indol-3-yl)-N-(1H-indol-3-ylmethyleneamino)methanimine

The solubility of the compound 1-(1H-indol-3-yl)-N-(1H-indol-3-ylmethyleneamino)methanimine is a noteworthy topic in the study of chemical properties. In general, the solubility of a compound can be influenced by various factors, including its molecular structure, polarity, and the solvent involved. For this particular compound, several points can be highlighted:

  • Polarity: The presence of multiple indole groups might suggest a level of hydrophobicity, potentially reducing solubility in polar solvents such as water.
  • Hydrogen Bonding: The compound may participate in hydrogen bonding interactions, which could lead to increased solubility in solvents that can form hydrogen bonds.
  • Solvent Compatibility: It is likely more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), rather than in aqueous solutions.

As a general rule, *“like dissolves like,”* meaning that polar compounds tend to be more soluble in polar solvents, and non-polar compounds are more soluble in non-polar solvents. For 1-(1H-indol-3-yl)-N-(1H-indol-3-ylmethyleneamino)methanimine, one may need to conduct experimental assays to precisely determine its solubility profile across various solvents.

Interesting facts

Interesting Facts about 1-(1H-indol-3-yl)-N-(1H-indol-3-ylmethyleneamino)methanimine

This intriguing compound, with its complex name, is a derivative of indole, a significant building block in organic chemistry known for its role in many natural products and pharmaceuticals. As a scientist or chemistry student, you'll find several fascinating aspects about this compound that showcase its potential and relevance in the field:

  • Biological Significance: Indole derivatives are often associated with a variety of biological activities, making them of great interest in medicinal chemistry. This compound may exhibit properties that could be explored for use in treating various diseases.
  • Chemical Versatility: The presence of amino and methylene functionality in this compound indicates its potential for further chemical transformations. This versatility can lead to the synthesis of various other important compounds.
  • Research Applications: The structural complexity of this molecule often encourages its study in pharmacological and toxicological research. It could serve as a lead compound in drug discovery that impacts signaling pathways in cells.
  • Indole Motif: The indole structure is a key feature in many natural alkaloids, suggesting that this compound may have applications in developing new materials or biochemical probes.
  • Interdisciplinary Connections: The study of this compound can bridge chemistry with biology and medicine, underscoring the importance of multidisciplinary approaches in scientific research.

While research on this specific compound is ongoing, the potential implications of its properties could play a significant role in future advancements in fields such as pharmacology, materials science, and beyond. As you delve deeper into the realm of chemical compounds, keep an eye on how structures like this can yield groundbreaking discoveries!

Synonyms
INDOLE-3-CARBOXALDEHYDE AZINE
654-638-5
1-(1H-Indol-3-yl)-N-(1H-indol-3-ylmethylideneamino)methanimine
MLS003106559
SCHEMBL3349880
CHEMBL1906165
DTXSID50924444
3-[(E)-[(2E)-2-[(1H-indol-3-yl)methylidene]hydrazin-1-ylidene]methyl]-1H-indole
AKOS024332277
SMR001821456
1,4-bis(3-indolyl)-2,3-diaza-1,3-butadiene
3,3'-(Hydrazinediylidenedimethanylylidene)di(1H-indole)