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3,4-Dichloromaleimide

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Identification
Molecular formula
C4HCl2NO2
CAS number
18835-51-1
IUPAC name
3,4-dichloropyrrole-2,5-dione
State
State

Under standard conditions, this compound is a solid. It has a crystalline form and maintains its integrity at room temperature, which is typically around 20 to 25 degrees Celsius.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.50
General information
Molecular weight
176.95g/mol
Molar mass
176.9520g/mol
Density
1.7280g/cm3
Appearence

3,4-Dichloromaleimide usually appears as a white to off-white crystalline solid. It can exist in powder form and tends to be quite stable under normal conditions, though it should be handled in a controlled environment to prevent any decomposition or unwanted reactions.

Comment on solubility

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

3,4-Dichloropyrrole-2,5-dione, an organic compound with intriguing chemical properties, exhibits notable characteristics when it comes to solubility. Understanding its solubility profile is essential for various applications in chemical synthesis and industrial processes.

Solubility Behavior

  • Solvent Polarity: This compound tends to show greater solubility in polar solvents such as water and dimethyl sulfoxide (DMSO) due to its ability to engage in hydrogen bonding.
  • Non-polar Solvent Interaction: In non-polar solvents, 3,4-dichloropyrrole-2,5-dione generally exhibits lower solubility, which could be attributed to its structural attributes that favor interactions with polar environments.

Key Points

  • Temperature Influence: Solubility is often temperature-dependent, typically increasing with higher temperatures, allowing for greater intermolecular interactions.
  • pH Considerations: The solubility may also vary with pH, influenced by the ionizable groups present in the compound, which can affect its overall ionization in solution.

In conclusion, the solubility of 3,4-dichloropyrrole-2,5-dione is a critical factor that influences its behavior in chemical processes. As one researcher noted, “Understanding the solubility parameters of this compound is vital for maximizing its utility in both laboratory and industrial settings.”

Interesting facts

Interesting Facts About 3,4-Dichloropyrrole-2,5-dione

3,4-Dichloropyrrole-2,5-dione, also known as a derivative of pyrrole, is a fascinating compound in the world of organic chemistry. Here are some key points to consider:

  • Versatile Intermediate: This compound serves as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure makes it a valuable building block in medicinal chemistry.
  • Reactivity: The presence of chlorine atoms enhances the reactivity of 3,4-dichloropyrrole-2,5-dione, allowing it to undergo various chemical transformations. This reactivity is useful in creating more complex molecules and exploring new reactions.
  • Biological Activity: Some derivatives of pyrrole compounds are known to exhibit interesting biological activities, including antimicrobial and anticancer properties. Researchers are continually investigating the potential of this compound in the pharmaceutical domain.
  • Environmental Aspect: The stability of this compound makes it a subject of study regarding environmental persistence, which is essential when considering the ecological impact of its use in various applications.
  • Research Significance: Studies on 3,4-dichloropyrrole-2,5-dione have expanded our understanding of nitrogen-containing heterocycles, contributing valuable insights into their chemistry, properties, and applications in advanced materials science.

As the field of organic chemistry continues to evolve, compounds like 3,4-dichloropyrrole-2,5-dione stand at the forefront of important research and development. Its potential applications in various industries highlight the necessity of in-depth exploration of such compounds.

Synonyms
3,4-dichloro-2,5-dihydro-1H-pyrrole-2,5-dione
873-408-7
1193-54-0
3,4-Dichloro-1H-pyrrole-2,5-dione
Dichloromaleimide
3,4-dichloropyrrole-2,5-dione
3,4-Dichloromaleimide
3,4-DICHLOROMALEINIMIDE
Dichloromaleinimide
1H-Pyrrole-2,5-dione, 3,4-dichloro-
MFCD01716135
alpha, beta-Dichloromaleimide
6G6K57D4OT
MALEIMIDE, DICHLORO-
CCRIS 7521
C4HCl2NO2
Maleimide, 2,3-dichloro-
BRN 0120989
UNII-6G6K57D4OT
Dichloro-Maleimide
O-(3,4-Dichlorobenzyl)hydroxylamine Hydrochloride; 3,4-Dichlorobenzyloxyamine Hydrochloride
SCHEMBL164583
SCHEMBL17962607
DTXSID30152405
CHEBI:184738
BAA19354
AKOS006279867
SB62033
AS-58001
SY124723
3,4-Dichloro-5-hydroxy-2H-pyrrol-2-one
DB-240761
CS-0037546
EN300-246596
W12239
Q27264854
Z1198158072