Skip to main content

Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C11H15NO3
CAS number
1119-42-6
IUPAC name
ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate
State
State

At room temperature, ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate is typically found in a liquid state.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
223.27g/mol
Molar mass
223.2650g/mol
Density
1.1200g/cm3
Appearence

Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate typically appears as a colorless to pale yellow liquid. It may also manifest in a crystalline solid form under specific conditions.

Comment on solubility

Solubility of Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate

Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate showcases intriguing solubility characteristics, which are important for its application in various chemical processes. Understanding the solubility of this compound can be defined by several key factors:

  • Polarity: The presence of both a carboxylate group and the ethyl ester functional group contributes to a level of polarity that affects solubility in different solvents.
  • Solvent compatibility: Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate is likely to be soluble in polar organic solvents such as ethyl acetate and possibly methanol, while being less soluble in non-polar solvents.
  • Temperature influence: Like many organic compounds, solubility may increase with temperature, making it essential to consider thermal conditions in practical applications.
  • Hydrogen bonding: The potential for hydrogen bonding due to the carboxylate group can enhance solubility in polar solvents, which aid in dissolution.

In summary, when evaluating the solubility of ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate, it is crucial to consider its chemical structure and functional groups, which collectively influence how this compound interacts with various solvents. The compatibility with polar and some semi-polar solvents highlights its potential uses in different chemical applications.

Interesting facts

Interesting Facts about Ethyl 5-Acetyl-2,4-Dimethyl-1H-Pyrrole-3-Carboxylate

This fascinating compound belongs to the pyrrole class of organic chemicals, known for their unique five-membered ring structure containing a nitrogen atom. Ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate has garnered interest in several fields, including pharmaceuticals and materials science.

Key Features:

  • Pharmacological Interest: Compounds related to pyrroles often exhibit biological activities. This molecule’s structure suggests potential applications in drug development, particularly as a lead structure for designing new therapeutic agents.
  • Synthesis Versatility: The synthetic pathways leading to the formation of this compound can be varied, allowing chemists to explore different reaction conditions and types of reagents. Such versatility boosts its potential for use in diverse synthetic applications.
  • Reactivity: The presence of both carboxylate and acetyl functionalities enhances its reactivity, making it a valuable intermediate in organic synthesis, particularly for constructing more complex molecular architectures.
  • Colorful Chemistry: While this specific compound might not have a colorful appearance, many pyrrole derivatives are known for their deep hues and are used in dyes and pigments.

Moreover, the pyrrole skeleton is a critical component in nature, appearing in various biological systems, including hemoglobin and chlorophyll. As a science student or a chemist, studying compounds like ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate opens the door to a deeper understanding of both organic chemistry and its real-world applications.

In the words of famed chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Thus, exploring such unique compounds enriches the creative avenues available in research and innovation.

Synonyms
ethyl 5-acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylate
877-613-2
6314-22-3
5-Acetyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester
5-acetyl-2,4-dimethyl-pyrrole-3-carboxylicaciethylester
PYRROLE-3-CARBOXYLIC ACID, 5-ACETYL-2,4-DIMETHYL-, ETHYL ESTER
NSC 40232
NSC 63924
BRN 0160846
5-Acetyl-2,4-dimethyl-pyrrole-3-carboxylic acid ethyl ester
MFCD00227068
NCIOpen2_002704
4-22-00-03003 (Beilstein Handbook Reference)
MLS000111867
SCHEMBL5203823
CHEMBL1496423
DTXSID00212484
ZCNAULQFSXEJTD-UHFFFAOYSA-N
HMS2401G21
ALBB-006667
NSC40232
NSC63924
NSC-40232
NSC-63924
STK502095
AKOS000266571
AB04987
LS-02367
SMR000107786
CS-0207389
EN300-04338
G29267
SR-01000389009
SR-01000389009-1
Z56862733
1H-Pyrrole-3-carboxylic acid, 5-acetyl-2,4-dimethyl-, ethyl ester