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3,4-Dimethylmaleimide

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Identification
Molecular formula
C6H7NO2
CAS number
1121-89-7
IUPAC name
3,4-dimethylpyrrole-2,5-dione
State
State

At room temperature, 3,4-Dimethylmaleimide is generally found in a solid state. Its crystalline form makes it easy to handle in laboratory and industrial settings where it is most commonly used.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
123.13g/mol
Molar mass
123.1430g/mol
Density
1.1700g/cm3
Appearence

3,4-Dimethylmaleimide typically appears as a crystalline solid. It can manifest in forms that range from colorless to slightly off-white, depending on purity and specific environmental conditions. The solid is typically formed into crystals or a crystalline powder that is fairly stable under standard storage conditions.

Comment on solubility

Solubility of 3,4-Dimethylpyrrole-2,5-dione

3,4-Dimethylpyrrole-2,5-dione, often referred to as a derivative of pyrrole, exhibits notable solubility characteristics. Here are some key points regarding its solubility:

  • Solvent Interaction: This compound tends to be soluble in polar solvents such as water, methanol, and ethanol, due to its ability to form hydrogen bonds with solvent molecules.
  • Nonpolar Solubility: In nonpolar solvents, the solubility can be limited. This is typical for many organic compounds with polar functional groups.
  • Temperature Dependence: The solubility of 3,4-dimethylpyrrole-2,5-dione may increase with temperature, as is the case with many organic compounds.
  • Concentration Factors: At higher concentrations, saturation may occur, impacting the effective solubility in solution.

In summary, while 3,4-dimethylpyrrole-2,5-dione demonstrates a good affinity for polar solvents, its solubility behavior is influenced by factors such as solvent choice and temperature. Understanding these interactions is crucial for practical applications in chemical processes.

Interesting facts

Interesting Facts about 3,4-Dimethylpyrrole-2,5-dione

3,4-Dimethylpyrrole-2,5-dione is a fascinating organic compound that belongs to the class of pyrrole derivatives. Known for its versatile reactivity and unique structure, this compound provides a rich ground for research and application in various fields.

Key Points of Interest:

  • Biological Significance:
    This compound is essential in the synthesis of various natural products, including important pharmaceuticals and agrochemicals. Its derivatives often display biological activity, making them valuable for medicinal chemistry.
  • Synthetic Applications:
    As a building block, 3,4-dimethylpyrrole-2,5-dione can be utilized in the synthesis of more complex molecules through various chemical reactions such as electrophilic aromatic substitution and nucleophilic additions.
  • Colorimetric Properties:
    The compound exhibits interesting colorimetric properties, leading to its potential use as a dye or indicator in analytical chemistry. This attribute is particularly useful in the detection of specific ions or molecules.
  • Insights into Reactivity:
    Its electronic structure plays a significant role in its reactivity, allowing chemists to predict and manipulate reactions involving this compound effectively.
  • Further Research:
    Scientists are continuously exploring the potential applications of 3,4-dimethylpyrrole-2,5-dione in areas like materials science and agriculture, seeking to uncover innovative uses that may benefit various industries.

In summary, 3,4-dimethylpyrrole-2,5-dione is not only an intriguing compound in organic chemistry but also a pivotal player with promising applications across multiple disciplines. Its properties embody the intersection of structure, function, and utility that continue to inspire chemists and researchers alike.

Synonyms
17825-86-4
2,3-DIMETHYLMALEIMIDE
3,4-dimethylpyrrole-2,5-dione
3,4-Dimethyl-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 3,4-dimethyl-
3,4-dimethyl-2,5-dihydro-1H-pyrrole-2,5-dione
dimethylmaleimide
56B9BV5BAR
dimethylmaleinimide
UNII-56B9BV5BAR
SCHEMBL181252
SCHEMBL1420924
SCHEMBL28765079
DTXSID70170446
ZTWMBHJPUJJJME-UHFFFAOYSA-N
SAA82586
AKOS012570573
AT29626
DB-356632
CS-0264639
EN300-93601
Z1117886924
InChI=1/C6H7NO2/c1-3-4(2)6(9)7-5(3)8/h1-2H3,(H,7,8,9