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2,3,5-Trimethylpyrrole

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Identification
Molecular formula
C7H11N
CAS number
13115-33-8
IUPAC name
2,3,5-trimethyl-1H-pyrrole
State
State

At room temperature, it is typically found as a liquid due to its relatively low melting point. Its state is maintained by its chemical structure and intermolecular forces.

Melting point (Celsius)
-82.00
Melting point (Kelvin)
191.15
Boiling point (Celsius)
174.00
Boiling point (Kelvin)
447.15
General information
Molecular weight
109.17g/mol
Molar mass
109.1690g/mol
Density
0.9162g/cm3
Appearence

2,3,5-Trimethyl-1H-pyrrole is a colorless to pale yellow liquid. It has a distinct sweet odor reminiscent of pyrrole derivatives.

Comment on solubility

Solubility of 2,3,5-trimethyl-1H-pyrrole

2,3,5-trimethyl-1H-pyrrole is an intriguing organic compound that displays notable solubility characteristics. Its solubility can be influenced by several factors:

  • Polarity: Due to the presence of nitrogen in its structure, the compound exhibits a certain degree of polarity, making it soluble in polar solvents.
  • Solvent Interaction: It is generally more soluble in organic solvents like ethanol, acetone, and chloroform.
  • Temperature: Solubility may also increase with temperature, which is a common trend for many organic compounds.

The dissolving behavior can be summarized as follows:

  • High solubility in alcohols and ethers
  • Limited solubility in water due to low hydrogen bonding capability

As a quoted observation, researchers often note: "The unique structure of pyrrole derivatives provides them with interesting solubility properties." Thus, understanding the solubility of 2,3,5-trimethyl-1H-pyrrole is crucial for its applications in various fields including chemistry and material science.

Interesting facts

Interesting Facts About 2,3,5-Trimethyl-1H-pyrrole

2,3,5-trimethyl-1H-pyrrole is an intriguing compound that belongs to the family of pyrroles, which are five-membered aromatic heterocycles containing nitrogen. Here are some fascinating insights about this compound:

  • Biological Relevance: Pyrrole derivatives, including 2,3,5-trimethyl-1H-pyrrole, play important roles in various biological processes. They are found in numerous natural products, such as chlorophyll, which is essential for photosynthesis in plants.
  • Flavor and Fragrance: This compound is known for contributing to the complex flavor profiles in certain foods. Its pleasant aroma makes it a candidate for use in the food and fragrance industries, highlighting its potential for enhancing sensory experiences.
  • Synthetic Versatility: 2,3,5-trimethyl-1H-pyrrole can serve as a building block in organic synthesis. Its unique structure allows for a variety of reactions, making it valuable in the development of more complex organic molecules.
  • Applications in Medicine: Some pyrrole compounds have been investigated for their pharmacological properties. This raises potential interest in exploring 2,3,5-trimethyl-1H-pyrrole for its effects on biological systems and its therapeutic possibilities.
  • Chemical Stability: The pyrrole ring, due to its aromatic nature, often exhibits a degree of chemical stability. This characteristic can be beneficial in designing compounds with specific desired properties or reactivities.

As a compound of scientific interest, 2,3,5-trimethyl-1H-pyrrole illustrates the rich diversity of organic molecules and their significance across various fields, from agriculture to medicinal chemistry.

Synonyms
2,3,5-TRIMETHYL-1H-PYRROLE
2199-41-9
1H-Pyrrole, 2,3,5-trimethyl-
DTXSID0073954
NSC 211492
DTXCID7036587
973-451-2
2,3,5-trimethylpyrrole
NSC211492
SCHEMBL33270
1H-Pyrrole,3,5-trimethyl-
2,3,5-trimethyl-1H-pyrrol
pyrrole, 2,3,5-trimethyl-
VIDOWPWTFHJVID-UHFFFAOYSA-N
2,3,5-Trimethyl-1H-pyrrole #
NSC-211492
EN300-102914