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1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone

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Identification
Molecular formula
C9H13NO
CAS number
25312-97-6
IUPAC name
1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone
State
State

The compound is usually found in a liquid state at room temperature.

Melting point (Celsius)
10.00
Melting point (Kelvin)
283.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
151.21g/mol
Molar mass
151.2100g/mol
Density
0.9978g/cm3
Appearence

This compound typically appears as a colorless to light yellow liquid.

Comment on solubility

Solubility of 1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone

The solubility of 1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone can be discussed in terms of its interactions with solvents and its structural properties. Here are some key points to consider:

  • Polarity: The presence of the pyrrole ring contributes to the overall polarity of the molecule, affecting its solubility in polar vs. nonpolar solvents.
  • Solvent Compatibility: This compound is expected to be soluble in organic solvents such as ethanol and dichloromethane, while showing limited solubility in water due to the hydrophobic characteristics of the alkyl groups.
  • Hydrogen Bonding: Interaction with solvents can be influenced by the ability to form hydrogen bonds. The nitrogen in the pyrrole ring may participate in hydrogen bonding, enhancing solubility in suitable solvents.

As stated in solubility theory, "like dissolves like." Thus, the solubility behavior of 1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone can largely be predicted based on the structure and functional groups present. Its solubility profile plays a crucial role in applications within pharmaceuticals and organic synthesis.

Interesting facts

Interesting Facts about 1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone

1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethanone is an intriguing compound that showcases the fascinating world of heterocyclic chemistry. This compound features a pyrrole ring, which is a five-membered aromatic ring containing nitrogen that contributes to its unique chemical behavior. Here are some interesting aspects of this compound:

  • Natural Occurrence: Pyrrole derivatives are commonly found in various natural products, including pharmaceuticals and vitamins, making them significant in both ecological and medicinal contexts.
  • Biological Activities: Compounds similar to this one have been studied for their potential pharmacological properties, which may include antibacterial, antifungal, and anticancer activities.
  • Versatile Building Blocks: The structure of this compound allows it to be used as a building block in organic synthesis, facilitating the design and development of more complex chemical entities.
  • Odor and Flavor: Pyrrole derivatives, including this compound, often contribute to the aroma profiles of various foods and fragrances, highlighting their importance in flavor chemistry.
  • Research Potential: Ongoing research aims to explore the synthesis and reactivity of such compounds, which could lead to exciting discoveries in the realms of material science and synthetic biology.

This compound is a testament to the creativity and utility of organic chemistry, embodying both the complexities of natural substances and the innovation of synthetic methodologies. As chemists continue to explore the functionalities of pyrrole-based compounds, we can anticipate novel applications that push the boundaries of science and technology.

Synonyms
19005-95-9
3-acetyl-2,4,5-trimethylpyrrole
3-Acetyl-2,4,5-trimethyl-pyrrole
KETONE, METHYL 2,4,5-TRIMETHYLPYRROL-3-YL
Methyl 2,4,5-trimethylpyrrol-3-yl ketone
W5UKK6E72S
BRN 0112922
1-(2,4,5-trimethyl-1H-pyrrol-3-yl)ethan-1-one
DTXSID10172469
5-21-07-00249 (Beilstein Handbook Reference)
DTXCID8094960
855-908-7
1-(2,4,5-Trimethyl-1H-pyrrol-3-yl)ethanone
Ethanone, 1-(2,4,5-trimethyl-1H-pyrrol-3-yl)-
792847-60-0
Methyl(2,4,5-trimethyl-1H-pyrrol-3-yl) ketone
(E)-1-(2,4,5-Trimethyl-3H-pyrrol-3-ylidene)ethan-1-ol
UNII-W5UKK6E72S
SCHEMBL8145766
3-Acetyl-2,4,5-trimethylpyrrol
XVBRWTVSTZYJIB-UHFFFAOYSA-N
MFCD01119094
STK396601
AKOS005431441
NCGC00326087-01
Methyl 2,4,5-trimethyl-3-pyrryl ketone
DB-286790
ST50862583
1-(Trimethyl-3H-pyrrol-3-ylidene)ethan-1-ol
EN300-213537
AB01321858-02
1-(2,4,5-Trimethyl-1H-pyrrol-3-yl)ethanone #
Q27292358
ETHANOL, 1-(2,4,5-TRIMETHYL-3H-PYRROL-3-YLIDENE)-