Interesting facts
Interesting Facts about 1-(1H-pyrrol-2-yl)ethanone
1-(1H-pyrrol-2-yl)ethanone is a fascinating compound that presents a unique blend of aromatic and heterocyclic chemistry. Here are some intriguing highlights about this molecule:
- Structural Composition: This compound features a pyrrole ring, which is a five-membered ring containing four carbon atoms and one nitrogen atom. The presence of nitrogen introduces diverse reactivity profiles and unique properties.
- Biological Activity: Compounds containing pyrrole structures are often investigated for their biological activity. Many derivatives have shown promising potential in pharmaceutical applications, particularly in areas like anti-cancer research.
- Flavor and Fragrance: Pyrrole derivatives, including 1-(1H-pyrrol-2-yl)ethanone, are sometimes associated with distinctive odors, which can be reminiscent of roasted coffee or chocolate. This aspect can lead to their use in flavorings and perfumes.
- Applications in Organic Synthesis: The presence of the pyrrole moiety allows for interesting synthetic pathways, often utilized in organic synthesis to create more complex molecules. Chemists value such compounds for their versatility and adaptability in creating novel materials.
- Research Interest: Ongoing research about the reactivity of 1-(1H-pyrrol-2-yl)ethanone is expanding. Scientists are studying its interactions and transformations, making it a subject of great interest in the fields of organic chemistry and material sciences.
In summary, 1-(1H-pyrrol-2-yl)ethanone is not only a compound of interest due to its structural features but also due to its potential applications and biological activities. As researchers continue to explore its capabilities, this compound may contribute to advancements in chemistry and related disciplines.
Synonyms
2-ACETYLPYRROLE
1072-83-9
1-(1H-Pyrrol-2-yl)ethanone
1-(1H-Pyrrol-2-yl)ethan-1-one
2-Pyrrolylethanone
Methyl pyrrol-2-yl ketone
2-Acetyl-1H-pyrrole
Ethanone, 1-(1H-pyrrol-2-yl)-
Ketone, methyl pyrrol-2-yl
2-Pyrrolyl methyl ketone
Methyl 2-pyrrolyl ketone
1-(2-Pyrrolyl)-1-ethanone
PYRROLE-B-METHYL KETONE
FEMA No. 3202
1-(1H-pyrrole-2-yl)-ethanone
1-(1H-pyrrol-2-yl)1-ethanone
Pyrrole-alpha-methyl ketone
CCRIS 6778
CHEBI:59981
EINECS 214-016-2
NSC 42861
BRN 0001882
9K28W7PM6N
DTXSID0047084
NSC-42861
2-ACETYLPYRROLE [FCC]
DTXCID8027084
5-21-07-00204 (Beilstein Handbook Reference)
METHYL 2-PYRROLYL KETONE [FHFI]
methyl pyrrolyl ketone
214-016-2
inchi=1/c6h7no/c1-5(8)6-3-2-4-7-6/h2-4,7h,1h
2-acetyl pyrrole
1-(1h-pyrrol-2-yl)-ethanone
MFCD00005220
Pyrrole, 2-acetyl
Methyl 2-pyrryl ketone
1H-Pyrrole, 2-acetyl
UNII-9K28W7PM6N
2-Acetopyrrole
2-acetyl-pyrrole
Pseudoacetylpyrrole
2-Acetyl-1H-indole
Spectrum2_001956
Spectrum3_001993
Pyrryl-alpha-methyl ketone
Epitope ID:136036
BSPBio_003593
SPECTRUM240422
Pyrrole-.alpha.-methyl ketone
SCHEMBL150349
SPBio_002051
SCHEMBL8153085
CHEMBL1414126
FEMA 3202
KBio3_003031
1-(1H-Pyrrol-2-yl)ethanone #
NSC42861
2-Acetylpyrrole, analytical standard
Ethanone, 1-(1H-pyrrole-2-yl)-
Tox21_300952
BBL010104
CCG-39485
STK801458
1-(1H-Pyrrol-2-yl)ethanone, 9CI
AKOS000120308
BS-3734
CS-W013672
HY-W012956
SB63880
SDCCGMLS-0066967.P001
2-Acetylpyrrole, ReagentPlus(R), 99%
Methyl 2-pyrrolyl ketone, >=98%, FG
NCGC00095914-01
NCGC00095914-02
NCGC00095914-03
NCGC00254854-01
PD002086
SY011279
CAS-1072-83-9
1-(1H-pyrrol-2-yl)ethanone (acetylpyrrole)
A0894
NS00020922
EN300-17239
F14878
2-Acetylpyrrole, Vetec(TM) reagent grade, 98%
AI-942/25034253
SR-05000002372
SR-05000002372-1
Q27127005
Z56899162
F8889-9291
Solubility of 1-(1H-pyrrol-2-yl)ethanone
1-(1H-pyrrol-2-yl)ethanone, also known as 2-acetylpyrrole, exhibits intriguing solubility properties that are influenced by its molecular structure. Being a heterocyclic compound, it possesses both hydrophobic and hydrophilic characteristics. Below are some key points regarding its solubility:
Overall, understanding the solubility of 1-(1H-pyrrol-2-yl)ethanone is crucial in fields such as organic synthesis and medicinal chemistry, as it affects both the reaction conditions and the effectiveness of the compound in various applications. As noted, solubility can vary significantly based on the solvent used, making it essential to select the appropriate medium for optimal results. Regular assessments and adjustments based on experimental conditions are advisable to maximize solubility.