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2,2'-Dipyrrolylmethanone

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Identification
Molecular formula
C9H8N2O
CAS number
7483-61-6
IUPAC name
di(pyrrol-1-yl)methanone
State
State

At room temperature, di(pyrrol-1-yl)methanone is a solid.

Melting point (Celsius)
44.00
Melting point (Kelvin)
317.00
Boiling point (Celsius)
415.20
Boiling point (Kelvin)
688.40
General information
Molecular weight
132.17g/mol
Molar mass
132.1570g/mol
Density
1.2260g/cm3
Appearence

Di(pyrrol-1-yl)methanone typically presents as a pale yellow or off-white solid. Its appearance is generally powdery and crystalline.

Comment on solubility

Solubility of di(pyrrol-1-yl)methanone

Di(pyrrol-1-yl)methanone, with its unique structure, presents interesting solubility characteristics that are governed by several factors:

  • Dipolar Nature: The presence of nitrogen atoms in the pyrrole rings contributes to its dipolar nature, potentially enhancing solubility in polar solvents.
  • Hydrogen Bonding: The compound's ability to participate in hydrogen bonding can facilitate solubility in protic solvents like water and alcohols.
  • Solvent Compatibility: Di(pyrrol-1-yl)methanone is generally more soluble in organic solvents such as dichloromethane and ethanol, rather than non-polar solvents, due to its polar characteristics.

However, it is important to note that precise solubility data can vary based on temperature and specific solvent interactions. As with many organic compounds, the rule of thumb is that “like dissolves like”; thus, polar compounds like di(pyrrol-1-yl)methanone are best dissolved in polar solvents.

In conclusion, while di(pyrrol-1-yl)methanone exhibits reasonable solubility in certain environments, the specific conditions should always be considered for optimal results.

Interesting facts

Exploring Di(pyrrol-1-yl)methanone

Di(pyrrol-1-yl)methanone is a fascinating compound that garners attention in the field of organic chemistry, especially for its unique structural features and versatile reactivity. Here are some intriguing facts about this compound:

  • Versatile Building Block: Di(pyrrol-1-yl)methanone serves as a key building block in the synthesis of various functional materials, including polymers and pharmaceuticals.
  • Unique Nitrogen-Containing Heterocycles: The pyrrole rings in the structure of di(pyrrol-1-yl)methanone contribute to its distinct electronic properties, making it an essential component in the development of organic semiconductors.
  • Biological Significance: Compounds similar to di(pyrrol-1-yl)methanone have shown potential biological activity, which could lead to exciting applications in drug discovery and development.
  • Reactivity: The compound exhibits interesting reactivity patterns typical of carbonyl-containing compounds, allowing it to participate in various chemical reactions such as nucleophilic additions and cycloadditions.
  • Research Interest: Scientists are actively researching di(pyrrol-1-yl)methanone and its derivatives, investigating their potential applications in fields ranging from materials science to medicinal chemistry.

As a scholar in chemistry, one cannot help but appreciate the intricate balance of structure and function exhibited by di(pyrrol-1-yl)methanone. Its ability to engage in diverse chemical transformations and its potential in practical applications underscore its importance in ongoing scientific research. In the words of one prominent chemist, "Every molecule tells a story; it is up to us to decipher its language."

In conclusion, di(pyrrol-1-yl)methanone is not just another compound; it is a versatile and promising player in the ever-evolving landscape of chemical research.

Synonyms
Dipyrrol-2-yl ketone
Di-1H-pyrrol-2-yl ketone
Ketone, di-1H-2-pyrrolyl
NSC 81355
BRN 0005216
5-24-03-00245 (Beilstein Handbook Reference)
Methanone, di-1H-pyrrol-2-yl-(9CI)
15770-21-5
Methanone, di-1H-pyrrol-2-yl-
Di(1H-pyrrol-1-yl)methanone
54582-33-1
N,N'-carbonylbisazole
1-(1H-pyrrole-1-carbonyl)-1H-pyrrole
2,2-Dipyrrolyl ketone
1,1'-Carbonyldipyrrole
di-1H-pyrrol-1-ylmethanone
SCHEMBL525220
9Z3N6NAS92
Methanone, di-1H-pyrrol-1-yl-
1H-Pyrrole, 1,1'-carbonylbis-
2,2'-Carbonylbis-(1H-pyrrole)
SB63691