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Phenylpyrrolylketone

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Identification
Molecular formula
C11H9NO
CAS number
932-16-1
IUPAC name
phenyl(1H-pyrrol-2-yl)methanone
State
State

At room temperature, Phenylpyrrolylketone is a solid.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
292.00
Boiling point (Kelvin)
565.15
General information
Molecular weight
171.20g/mol
Molar mass
171.1960g/mol
Density
1.1180g/cm3
Appearence

Phenylpyrrolylketone is a pale yellow solid compound. It is often found in crystalline form and demonstrates the typical aromatic odor associated with compounds containing a phenyl group.

Comment on solubility

Solubility of Phenyl(1H-pyrrol-2-yl)methanone

The solubility of phenyl(1H-pyrrol-2-yl)methanone can be influenced by several factors due to its unique chemical structure. Here are some key points regarding its solubility:

  • Polarity: The presence of both a phenyl and a pyrrol moiety suggests that the compound may exhibit moderate polarity. This can affect its solubility in various solvents.
  • Solvent Compatibility: Phenyl(1H-pyrrol-2-yl)methanone is likely to be soluble in organic solvents such as:
    • Ethanol
    • Acetone
    • Dichloromethane
  • Water Solubility: Its solubility in water is expected to be low, primarily due to the hydrophobic characteristics of the phenyl group.
  • Temperature Dependence: Generally, the solubility can increase with temperature, which is a common trait for organic compounds.
  • Effect of pH: If the substance has any potential acidic or basic functional groups, the solubility could vary with changes in pH.

In summary, while phenyl(1H-pyrrol-2-yl)methanone is likely to exhibit moderate solubility in organic solvents, its presence in aqueous solutions is generally limited. This insight can be crucial for applications in chemical synthesis and analysis.

Interesting facts

Interesting Facts about Phenyl(1H-pyrrol-2-yl)methanone

Phenyl(1H-pyrrol-2-yl)methanone is a fascinating compound that plays an important role in various fields of chemistry and pharmacology. Here are some key highlights:

  • Structural Features: This compound is characterized by a unique combination of a phenyl group and a pyrrole moiety. The pyrrole ring contributes to the compound's reactivity and potential biological activity.
  • Biological Significance: Compounds containing pyrrole are often found in many natural products and have been studied for their biological properties, including anti-inflammatory and anti-cancer activities.
  • Synthetic Versatility: The presence of two distinct functional groups allows for various synthetic pathways. Chemists can modify the structure to explore new derivatives with unique properties.
  • Applications in Material Science: Beyond organic chemistry, this compound and its derivatives are being investigated for their potential applications in organic electronics and as functional materials.

The study of phenyl(1H-pyrrol-2-yl)methanone embodies the essence of interdisciplinary research, bridging organic synthesis and pharmacological investigations, making it a worthy subject of study in modern chemical research.

In conclusion, the exploration of such compounds can lead to groundbreaking discoveries, emphasizing the importance of research in unearthing new applications and benefits for society.

Synonyms
phenyl(1H-pyrrol-2-yl)methanone
664-147-8
2-Benzoylpyrrole
7697-46-3
2-Benzoyl-1H-pyrrole
Methanone,phenyl-1H-pyrrol-2-yl-
Methanone, phenyl-1H-pyrrol-2-yl-
KETONE, PHENYL PYRROL-2-YL
Phenyl-1H-pyrrol-2-ylmethanone
MLS002693952
NSC-75585
Pyrrol-2-ylphenyl ketone
Phenyl pyrrol-2-yl ketone
NSC 75585
BRN 0120606
NSC75585
MFCD00094048
Maybridge3_006364
ChemDiv2_003108
8WB7U6L8VA
NCIOpen2_000432
5-21-08-00461 (Beilstein Handbook Reference)
SCHEMBL1074961
CHEMBL2136039
DTXSID80227753
NFGGQMYSOLVBLF-UHFFFAOYSA-N
HMS1377N06
HMS1449B06
HMS3079P21
phenyl-(1H-pyrrol-2-yl)-methanone
AC-106
CCG-42083
AKOS013059135
MB00640
IDI1_017751
AS-60987
SMR000031378
DB-313531
B4934
CS-0156555
SR-01000632111-1