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α-Pyrrolidinoheptaphyrin

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Identification
Molecular formula
C24H20N3O2
CAS number
101-83-7
IUPAC name
3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione
State
State

At room temperature, this compound exists in a solid state. It is primarily used in chemical research and may have specific handling requirements given its structural complexity.

Melting point (Celsius)
151.00
Melting point (Kelvin)
424.00
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.65
General information
Molecular weight
356.44g/mol
Molar mass
356.3380g/mol
Density
1.3400g/cm3
Appearence

The compound typically appears as a crystalline solid that is often pale yellow to off-white in color. As with many complex organic compounds, its exact appearance can vary slightly depending on purity and the exact conditions under which it was synthesized and isolated.

Comment on solubility

Solubility of 3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione

The compound 3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione, with the chemical formula C24H20N3O2, exhibits unique solubility characteristics that may influence its potential applications in various fields.

In general, solubility can be influenced by several factors:

  • Polarity: This compound contains both hydrophobic (indole) and hydrophilic (amino) functional groups, which may allow it to dissolve in a range of solvents.
  • Solvent type: Likely soluble in organic solvents such as methanol, DMSO, and ethanol, while displaying limited solubility in water due to its large non-polar sections.
  • Temperature: Increased temperature may enhance solubility, allowing better interaction of the compound with solvent molecules.

Furthermore, some experimental observations indicate that "solubility can change remarkably depending on the presence of other solutes or by altering pH." This implies that:

  • At neutral pH: Expected solubility will be relatively low.
  • In acidic or basic conditions: Solubility might improve due to ionization of amino groups, influencing interactions with solvents.

Overall, while solubility studies on this specific compound are limited, its structural complexity suggests potential for diverse solubility behavior, meriting further investigation. Understanding these solubility dynamics is crucial for optimizing its pharmaceutical or chemical applications.

Interesting facts

Exploring 3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione

This compound is a fascinating member of the indole family, known for its complex structure and potential biological activities. Indoles are well-studied due to their significant presence in many natural products and pharmaceuticals. Here are some interesting facts about this particular compound:

  • Structural Complexity: The compound features both indole and pyrrole groups, which contribute to its intriguing chemical reactivity and possible interaction mechanisms within biological systems.
  • Biological Relevance: Many indole-derived compounds are known to exhibit a variety of biological activities, including anticancer, anti-inflammatory, and antimicrobial effects. The presence of the amino group may further enhance its potential in medicinal chemistry.
  • Plausible Applications: Due to its structural characteristics, this compound could serve as a lead compound for the synthesis of novel therapeutic agents targeting various diseases, especially those related to neurobiology.
  • Research Interest: Scientists continue to explore indole compounds to understand their mechanisms of action at the cellular level, allowing for the development of better drugs with fewer side effects.
  • Derivative Potential: The ability to modify the indole moieties may lead to a diverse range of derivatives with tailored pharmacological profiles, expanding its application in drug discovery.

In conclusion, 3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione stands as a testament to the intricacies of organic chemistry, bridging the gap between structural design and functional application in therapeutic contexts. As research progresses, this compound may contribute to significant advancements in pharmacology and medicinal chemistry.

Synonyms
bisindolylmaleimide viii
125313-65-7
Ro 31-7549
3-[1-(3-AMINOPROPYL)-1H-INDOL-3-YL]-4-(1-METHYL-1H-INDOL-3-YL)-1H-PYRROLE-2,5-DIONE
Ro-31-7549
3-[1-(3-aminopropyl)indol-3-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione
Y6197FQK8I
DTXSID00154734
1H-Pyrrole-2,5-dione, 3-(1-(3-aminopropyl)-1H-indol-3-yl)-4-(1-methyl-1H-indol-3-yl)-
3-(1-(3-Aminopropyl)-1H-indol-3-yl)-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione
Ro 31-7549 (acetate);Bis VIII (acetate)
BI8
1H-Pyrrole-2,5-dione,3-(1-(3-aminopropyl)-1H-indol-3-yl)-4-(1-methyl-1H-indol-3-yl)-
1uvr
1H-Pyrrole-2,5-dione, 3-[1-(3-aminopropyl)-1H-indol-3-yl]-4-(1-methyl-1H-indol-3-yl)-
DTXSID50432099
Bis VIII
Bisindolylmaleimide VIII acetate salt
UNII-Y6197FQK8I
BIM-8
Bisindolylmaleimide deriv. 2b
BDBM2695
CHEMBL269264
SCHEMBL1942352
DTXCID0077225
DTXCID90382928
UQHKJRCFSLMWIA-UHFFFAOYSA-N
HMS3401F09
HSCI1_000320
NSC767216
DB01946
NSC-767216
SDCCGRCH-0000080.P001
SDCCGSBI-0640481.P001
NCGC00262036-03
DB-084858
HY-129624
CS-0107004
NS00068800
Q27093045
3-[1-(3-aminopropanyl)-3-indolyl]-4-(1-methyl-3-indolyl)-1 h pyrrole-2,5-dione
3-[1-(3-aminopropyl)-1H-indol-3-yl]-4-(1-methyl-1H-indol-3-yl)-2,5-dihydro-1H-pyrrole-2,5-dione