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3,4-Dichloro-1-methylpyrrole-2,5-dione

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Identification
Molecular formula
C5H3Cl2NO2
CAS number
38446-78-7
IUPAC name
3,4-dichloro-1-methyl-pyrrole-2,5-dione
State
State

At room temperature, 3,4-Dichloro-1-methylpyrrole-2,5-dione is in a solid state, generally appearing as white to off-white crystals.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.00
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.00
General information
Molecular weight
193.96g/mol
Molar mass
193.9610g/mol
Density
1.6500g/cm3
Appearence

3,4-Dichloro-1-methylpyrrole-2,5-dione appears as a crystalline solid, typically white to off-white in color. Its structure is comprised of a pyrrole ring with two chlorine atoms and a methyl group attached, giving it a distinctive shape that affects its physical properties.

Comment on solubility

Solubility of 3,4-Dichloro-1-methyl-pyrrole-2,5-dione

The solubility of the compound 3,4-dichloro-1-methyl-pyrrole-2,5-dione, also commonly identified by its systematic name, is an interesting topic due to its unique molecular structure. This compound exhibits variable solubility depending on the solvent and environmental conditions. Here are some key points regarding its solubility:

  • Polar Solvents: This compound tends to be more soluble in polar solvents due to its ability to interact with other polar molecules.
  • Non-Polar Solvents: In contrast, its solubility in non-polar solvents is generally low, indicating minimal interactions.
  • Temperature Effects: Increased temperature often enhances solubility for many organic compounds, and this compound may follow that trend.
  • pH Influence: The solubility may also be affected by the pH of the solution, as it can influence the ionization states of the compound.

As a rule of thumb: “Like dissolves like.” Therefore, it is essential to consider the polarity of both the solute and solvent when predicting solubility. Understanding the solubility characteristics of 3,4-dichloro-1-methyl-pyrrole-2,5-dione can be fundamental for its practical applications in various fields, including pharmaceuticals and materials science.

Interesting facts

Interesting Facts about 3,4-Dichloro-1-methyl-pyrrole-2,5-dione

3,4-Dichloro-1-methyl-pyrrole-2,5-dione, commonly known as a derivative of pyrrole, is a fascinating compound with several intriguing characteristics and applications. Here are some noteworthy points:

  • Biological Activity: This compound exhibits various biological activities, making it of interest in pharmaceutical research. It has potential uses in developing new drugs and therapies.
  • Coloring Agents: The presence of chlorinated groups in the structure contributes to its potential as a dye or pigment, highlighting its role in the coloring industry.
  • Environmental Impact: Understanding compounds like 3,4-dichloro-1-methyl-pyrrole-2,5-dione is crucial because of their persistence in the environment and potential ecological effects.
  • Reactivity: The unique structure allows for notable reactivity, especially in organic synthesis. It participates in a variety of chemical reactions, making it a valuable intermediate in synthetic pathways.
  • Research Applications: This compound is used in various research settings, particularly in studies focused on nitrogen-containing heterocycles, which play key roles in biological processes.

In conclusion, 3,4-dichloro-1-methyl-pyrrole-2,5-dione represents a rich area of study within organic chemistry, with implications spanning from industrial applications to environmental science. The continued exploration of its properties and reactions promises to unveil even more exciting possibilities!

Synonyms
2,3-Dichloro-N-methylmaleimide
3,4-dichloro-1-methylpyrrole-2,5-dione
601-181-4
1123-61-1
3,4-dichloro-1-methyl-1H-pyrrole-2,5-dione
Dichloro-N-methylmaleimide
N-Methyldichloromaleimide
3,4-dichloro-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione
N-Methyl-2,3-dichloromaleimide
Maleimide, dichloro-N-methyl-
N-Methyl-3,4-dichloromaleimide
2,3-Dichloro-N-methylmaleinimide
MALEIMIDE, 2,3-DICHLORO-N-METHYL-
1H-Pyrrole-2,5-dione, 3,4-dichloro-1-methyl-
NSC-222494
N-Methyldichloromaleinimide
n-Methyl-dichloromaleinimide
NSC 222494
BRN 0127988
MFCD00830725
NSC222494
3,4-dichloro-1-methyl-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione,3,4-dichloro-1-methyl-
D5ARQ6B32V
SCHEMBL407513
2,3-dichloro N-methylmaleimide
Maleimide,3-dichloro-N-methyl-
3,4-Dichloro-1-methylmaleimide
DTXSID80149981
WLZ3276
PYOLPWAVSYVLMM-UHFFFAOYSA-N
AKOS016014031
1H-Pyrrole-2, 3,4-dichloro-1-methyl-
DB-041080
CS-0242921
NS00023629
G51032
EN300-2568223
Z1255372921