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N-Phenylmaleimide

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Identification
Molecular formula
C10H5NO2
CAS number
941-69-5
IUPAC name
1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione
State
State

At room temperature, N-Phenylmaleimide is typically in a solid state. It is stable and retains its solid form under normal conditions.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
291.90
Boiling point (Kelvin)
565.05
General information
Molecular weight
185.16g/mol
Molar mass
185.1630g/mol
Density
1.3660g/cm3
Appearence

N-Phenylmaleimide is a yellow crystalline solid. It may also appear as pale yellow to off-white crystalline powder. The compound is often noted for its distinctive crystalline texture.

Comment on solubility

Solubility of 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione

The solubility of the compound 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione can be characterized by several key factors:

  • Polarity: This compound contains multiple functional groups that increase its polarity, likely enhancing its solubility in polar solvents.
  • Hydrogen Bonding: The presence of carbonyl (C=O) groups suggests that hydrogen bonding can occur, promoting solubility in water due to interactions with solvent molecules.
  • Solvent Dependency: It may exhibit variable solubility depending on the type of solvent. For instance, it is expected to be more soluble in dimethyl sulfoxide (DMSO) or dimethylformamide (DMF) compared to non-polar solvents.
  • Temperature Effects: As with many organic compounds, solubility could increase with temperature, facilitating dissolution.

In summary, while exact solubility data may vary, the compound's potential for solubility in polar solvents and temperature sensitivity makes it a subject of interest in solubility studies.

Interesting facts

Interesting Facts about 1-[3-(2,5-Dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione

This compound is a fascinating example of organic chemistry due to its multi-component structure and potential applications. Below are some intriguing aspects:

  • Biological Significance: Compounds like 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione are noted for their diverse biological activities. They have been studied for their potential roles in antimicrobial and antitumor activities.
  • Structural Complexity: The molecule contains a pyrrole ring and a dioxopyrrol structure, which makes it interesting for researchers investigating complex ring systems and their reactivity. This complexity leads to unique reactivity patterns that could be exploited in synthesis.
  • Potential in Dyes: Certain derivatives of pyrrole compounds are known for their vibrant colors and stability, leading to possible applications in dye chemistry. Research into similar compounds has opened avenues for sustainable dye production.
  • Material Science: Research indicates that these compounds could be utilized in material science, particularly in the synthesis of conductive polymers, which are essential in organic electronics.

In the words of a famous chemist, “Chemistry is the art of synthesis.” This compound exemplifies that art, showcasing how nature's building blocks can be employed to innovate and inspire.

With ongoing research, the exploration of this compound may yield further exciting discoveries, exemplifying how organic compounds can bridge multiple scientific disciplines.

Synonyms
3006-93-7
N,N'-1,3-Phenylenedimaleimide
m-Dimaleimidobenzene
m-Phenylenedimaleimide
m-Phenylenebismaleimide
1,3-Dimaleimidobenzene
N,N'-m-Phenylenedimaleimide
1,3-Bismaleimidobenzene
1,3-Phenylenebismaleimide
M-Phdm
HVA 2
HVA-2 curing agent
N,N'-m-Phenylenemaleimide
1H-Pyrrole-2,5-dione, 1,1'-(1,3-phenylene)bis-
N,N'-(m-Phenylene)bismaleimide
NSC 19639
N,N'-(m-Phenylenedimaleimide)
Maleimide, N,N'-m-phenylenedi-
EINECS 221-112-8
MD8KF155CT
1,1'-(m-Phenylene)bis-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 1,1'-(phenylene)bis-
BRN 0249503
1,1'-(1,3-Phenylene)bis-1H-pyrrole-2,5-dione
DTXSID3044415
N,N'-1,3-Phenylenebismaleimide
BMI-MP
NSC-19639
1,1'-(1,3-Phenylene)bis(1H-pyrrole-2,5-dione)
MALEIMIDE, N,N'-(m-PHENYLENE)DI-
n,n'-m-phenylenebis(maleimide)
DTXCID1024415
BMI 3000
mDimaleimidobenzene
MPhDM
HVA2 curing agent
mPhenylenedimaleimide
mPhenylenebismaleimide
1,3Dimaleimidobenzene
HVA2CURATIVE
1,3Bismaleimidobenzene
VANAX MBM PWDR
1,3Phenylenebismaleimide
N,N'(mPhenylenedimaleimide)
N,N'(mPhenylene)bismaleimide
N,N'1,3Phenylenedimaleimide
Maleimide, N,N'(mphenylene)di
N,N'(1,3Phenylene)dimaleimide
1,1'(mPhenylene)bis1Hpyrrole2,5dione
1,1'(1,3Phenylene)bis1Hpyrrole2,5dione
1,1'(mPhenylene)bis1Hpyrrole2,5dione (9CI)
1,1'-(m-Phenylene)bis-1H-pyrrole-2,5-dione (9CI)
N,N'-1,3-Phenylene bismaleimide
N,N-1,3-Phenylenedimaleimide
NN'-13-Phenylenedimaleimide
N.N-m-phenylene dimaleimide
1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione
N,N'-(1,3-Phenylene)dimaleimide
1-[3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)phenyl]-2,5-dihydro-1H-pyrrole-2,5-dione
phenyl-1,3-bismaleimide
CHEMBL573689
N,N-1,3-Phenylene bismaleimide
UNII-MD8KF155CT
N,N'-m-phenylene bismaleimide
N,N''-1,3-Phenylenedimaleimide
Vanax MBM
MFCD00022569
m-Phenylenedi(maleimide)
N,3-Phenylenedimaleimide
m-Phenylenebis(maleimide)
N,N'-m-Phenyledimaleimide
1,3-phenylene bismaleimide
Maleimide,N'-m-phenylenedi-
SCHEMBL94730
N,N'-Meta-phenylenedimaleimide
N,N'-1,3-Bismaleimidobenzene
BCP25887
N,N\'-1,3-Phenylene bismaleimide
NSC19639
Tox21_303753
WLN: T5VNVJ BR C- BT5VNVJ
BDBM50300347
GEO-03119
STK386206
AKOS004115393
N,N'-(Benzene-1,3-diyl)dimaleimide
FP07099
PS-5627
NCGC00356976-01
PD135224
CAS-3006-93-7
N,N'-(1,3-Phenylene)dimaleimide, 97%
DB-068208
CS-0156891
NS00019562
P0976
1H-Pyrrole-2, 1,1'-(1,3-phenylene)bis-
E81954
A820173
1,1'-benzene-1,3-diylbis(1H-pyrrole-2,5-dione)
Q27283915
1-[3-(2,5-dioxo-1-pyrrolyl)phenyl]pyrrole-2,5-dione
1-[3-[2,5-bis(oxidanylidene)pyrrol-1-yl]phenyl]pyrrole-2,5-dione
37453-16-0
InChI=1/C14H8N2O4/c17-11-4-5-12(18)15(11)9-2-1-3-10(8-9)16-13(19)6-7-14(16)20/h1-8