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Nicotine

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Identification
Molecular formula
C10H14N2
CAS number
54-11-5
IUPAC name
3-(1-methylpyrrolidin-2-yl)-1H-indole
State
State

Nicotine is a liquid at room temperature.

Melting point (Celsius)
-79.00
Melting point (Kelvin)
194.15
Boiling point (Celsius)
247.00
Boiling point (Kelvin)
520.15
General information
Molecular weight
162.23g/mol
Molar mass
162.2340g/mol
Density
1.0104g/cm3
Appearence

Nicotine is a clear to yellowish oily liquid at room temperature. It turns brown on exposure to air and emits a strong odor of tobacco.

Comment on solubility

Solubility of 3-(1-methylpyrrolidin-2-yl)-1H-indole

The solubility of 3-(1-methylpyrrolidin-2-yl)-1H-indole, a complex organic compound, is influenced by several factors:

  • Polarity: This compound exhibits a moderate level of polarity due to the presence of nitrogen atoms in its structure, which can interact with polar solvents.
  • Solvent Choice: Generally, 3-(1-methylpyrrolidin-2-yl)-1H-indole is likely to be more soluble in organic solvents such as ethanol or dichloromethane, compared to water, due to its hydrophobic aromatic ring.
  • Temperature: As with many organic compounds, increased temperature often enhances solubility, allowing for better interaction with the solvent at higher kinetic energy.

In conclusion, understanding the solubility of 3-(1-methylpyrrolidin-2-yl)-1H-indole is crucial for its applications in fields such as pharmaceuticals and material science. It is essential to consider both the chemical structure and the environment when determining how readily this compound will dissolve.

Interesting facts

Interesting Facts About 3-(1-methylpyrrolidin-2-yl)-1H-indole

3-(1-methylpyrrolidin-2-yl)-1H-indole is a fascinating compound that has garnered attention in various scientific fields due to its unique structure and potential applications. Here are some interesting aspects:

  • Chemical Structure: The compound features an indole moiety, which is a core structure in many biologically active compounds. This structure is known for its aromaticity and is often found in natural products, pharmaceuticals, and dyes.
  • Biological Activity: Research suggests that compounds containing the indole framework can exhibit diverse biological activities, including anti-inflammatory, analgesic, and anticancer properties, making this compound a subject of interest in medicinal chemistry.
  • Cognitive Enhancement Potential: The presence of the pyrrolidine ring indicates potential neuroactive effects. Studies into compounds with similar structures have shown promise in enhancing cognitive function and memory.
  • Research Applications: 3-(1-methylpyrrolidin-2-yl)-1H-indole is being investigated in various research areas, particularly in pharmacology and neurochemistry, as scientists look to explore its potential therapeutic effects.
  • Drug Development: As a member of a group of compounds known for their activity against certain types of diseases, it plays a role in the ongoing search for new therapies that can be utilized in treating conditions ranging from neurodegenerative diseases to mental health disorders.

The study of 3-(1-methylpyrrolidin-2-yl)-1H-indole exemplifies how a single compound can open doors to new therapeutic avenues and deepen our understanding of complex biological systems. As researchers continue to explore its mechanisms and potential uses, this compound may well become a crucial player in the development of future medications.

Synonyms
3-(1-Methyl-2-pyrrolidinyl)-1H-indole
111-974-2
3-(1-Methyl-2-pyrrolidinyl)indole
3-(1-methylpyrrolidin-2-yl)-1H-indole
INDOLE, 3-(1-METHYL-2-PYRROLIDINYL)-
7236-83-1
254KT5K2BQ
BRN 0611673
1H-Indole, 3-(1-methyl-2-pyrrolidinyl)-
UNII-254KT5K2BQ
Oprea1_713525
SCHEMBL13162093
DTXSID50993150
3-(1-methyl-2-pyrrolidyl)indole
AE-473/30364064