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N-Phthalimide

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Identification
Molecular formula
C8H4N2O4
CAS number
2216-57-3
IUPAC name
4-nitroisoindoline-1,3-dione
State
State

At room temperature, 4-nitroisoindoline-1,3-dione is a solid.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.00
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.00
General information
Molecular weight
192.14g/mol
Molar mass
192.1410g/mol
Density
1.5000g/cm3
Appearence

4-Nitroisoindoline-1,3-dione is typically a yellow crystalline solid. It appears as fine, needle-like crystals which are stable under normal conditions.

Comment on solubility

Solubility of 4-nitroisoindoline-1,3-dione

When considering the solubility of 4-nitroisoindoline-1,3-dione, also known as phthalimide, one must pay attention to several important factors that influence its behavior in various solvents. The compound has a unique structure that affects its solubility profile:

  • Polarity: The presence of the nitro group (-NO2) increases the polarity of the molecule, making it more soluble in polar solvents.
  • Solvent Interaction: 4-nitroisoindoline-1,3-dione tends to dissolve well in water and various organic solvents such as ethanol and acetone.
  • Temperature Dependence: As is common for many organic compounds, solubility can be significantly enhanced at elevated temperatures.

It can be summarized that:

  • Low solubility in non-polar solvents due to its relatively polar structure.
  • Moderate solubility in polar solvents, showcasing its capacity to interact with solvent molecules.
  • Temperature plays a pivotal role, indicating that solubility may vary with environmental conditions.

In conclusion, understanding the solubility characteristics of 4-nitroisoindoline-1,3-dione is crucial for applications in research and industry, particularly in pharmacology where solubility can directly impact bioavailability.

Interesting facts

Exploring 4-Nitroisoindoline-1,3-dione

4-Nitroisoindoline-1,3-dione is a fascinating compound with a rich history and significant applications in various fields of science. Here are some intriguing facts about this distinctive chemical:

  • Structure and Stability: The compound features a unique isoindoline structure, which contributes to its distinctive properties and stability in various chemical environments.
  • Biological Activity: Research has indicated that 4-nitroisoindoline-1,3-dione may exhibit notable biological activity, including potential therapeutic effects that are being explored in medicinal chemistry.
  • Role in Organic Synthesis: This compound serves as an essential intermediate in organic synthesis, facilitating the production of more complex molecules, particularly in the development of pharmaceuticals.
  • Innovative Research: Scientists are continuously uncovering new uses for this compound. Recent studies are focusing on its role in material science, especially in creating novel organic materials for electronics and sensors.
  • Sustainability Perspectives: As researchers push towards green chemistry, compounds like 4-nitroisoindoline-1,3-dione are also being looked at for their potential in creating environmentally friendly processes due to their reactivity and functionality.

As we delve deeper into the properties and applications of 4-nitroisoindoline-1,3-dione, it is evident that this compound not only supports existing scientific theories but also opens doors for innovative applications that can benefit various industries. "The next breakthrough in chemistry may just lie in understanding compounds like these more thoroughly."

Synonyms
3-NITROPHTHALIMIDE
603-62-3
Phthalimide, 3-nitro-
1H-Isoindole-1,3(2H)-dione, 4-nitro-
NL6BP8BS7W
NSC 5393
NSC-5393
EINECS 210-051-2
4-Nitro-1H-isoindole-1,3(2H)-dione
AI3-08841
DTXSID3060532
DM113
DM 113
DM-113
DTXCID5042790
210-051-2
4-nitroisoindole-1,3-dione
4-nitroisoindoline-1,3-dione
MFCD00041852
nitrophthalimide
4-nitro-2,3-dihydro-1H-isoindole-1,3-dione
4-nitro-isoindole-1,3-dione
3-nitro-phthalimide
UNII-NL6BP8BS7W
3-Nitrophthalimide, 97%
Oprea1_240526
1H-Isoindole-1, 4-nitro-
SCHEMBL284027
BONIIQYTWOPUQI-UHFFFAOYSA-
NSC5393
BCP27173
STK726722
AKOS000120865
AKOS025212234
CS-W019191
GS-3345
SB66103
AC-19447
SY003161
4-Nitro-1H-isoindole-1,3(2H)-dione #
EU-0034392
N0666
NS00034342
EN300-17066
SR-01000396410
SR-01000396410-1
Z56870733
InChI=1/C8H4N2O4/c11-7-4-2-1-3-5(10(13)14)6(4)8(12)9-7/h1-3H,(H,9,11,12)