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2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole

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Identification
Molecular formula
C26H26N2
CAS number
76437-29-1
IUPAC name
2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole
State
State

At room temperature, this compound remains a solid. The crystalline structure contributes to its stable form under standard conditions.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
505.80
Boiling point (Kelvin)
778.90
General information
Molecular weight
348.50g/mol
Molar mass
348.4640g/mol
Density
1.2110g/cm3
Appearence

This compound typically appears as an off-white to light brown solid. It may crystallize in a form that exhibits slight opacity.

Comment on solubility

Solubility of 2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole

The solubility of 2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole is an intriguing aspect of its chemical profile. One of the significant factors influencing its solubility includes:

  • Polarity: The compound contains both non-polar (aromatic rings) and polar (pyrrolidine) components, which can affect its solubility in various solvents.
  • Solvent Compatibility: Generally, it is anticipated to have higher solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and chloroform due to its organic nature.
  • Temperature Influence: As with many organic compounds, an increase in temperature can lead to increased solubility in solvents.

However, it is important to note that solubility data can vary based on specific conditions and require empirical measurement for precise determination. In terms of practical applications, understanding these solubility characteristics is crucial for utilizing this compound effectively in chemical synthesis or pharmaceutical formulations.

Interesting facts

Interesting Facts about 2,3-Diphenyl-1-(2-pyrrolidin-1-ylethyl)indole

2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole is a fascinating compound that combines elements of both **indole** and **pyrrolidine**, making it a valuable subject of study in various scientific disciplines.

Key Features of the Compound:

  • Diverse Applications: This compound has potential applications in pharmaceuticals, specifically in drug design and development due to its unique structural properties.
  • Structural Insights: Its structure consists of an indole ring, which is known for its role in many biological molecules, and a pyrrolidine moiety that can influence the compound's **bioactivity**.
  • Chirality Potential: The presence of the pyrrolidine group introduces chirality, which can significantly affect the pharmacological behavior of the compound. In drug development, chirality often plays a critical role in **selectivity** and **efficacy**.
  • Molecular Interactions: The diphenyl substitution on the indole ring enhances interactions with biological targets. Compounds with such structures often exhibit high affinity for specific receptors.

Researchers have been particularly interested in how this compound can interact with the **central nervous system**. As a derivative of indole, a core structure in many neurotransmitters, its potential effects on serotonin receptors make it an intriguing candidate for studies related to mood disorders.

Moreover, the interdisciplinary nature of studies involving this compound showcases the intersection of **organic chemistry**, **medicinal chemistry**, and **biochemistry**. The insights gained from exploring 2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole can pave the way for innovations in **targeted therapies**, an area that is gaining momentum in modern medicine.

In conclusion, 2,3-diphenyl-1-(2-pyrrolidin-1-ylethyl)indole is not just a chemical compound but a bridge leading to potential breakthroughs in drug development and therapeutic strategies. Its rich structural features and versatility make it a compound worth studying!

Synonyms
INDOLE, 2,3-DIPHENYL-1-(2-(1-PYRROLIDINYL)ETHYL)-
14036-25-0
BRN 1401512
1-beta-Pyrrolidinoethyl-2,3-diphenylindole
2,3-Diphenyl-1-(2-(1-pyrrolidinyl)ethyl)indole
5-20-08-00576 (Beilstein Handbook Reference)
DTXSID30161315