Interesting facts
Interesting Facts about 4-Nitroisobenzofuran-1,3-dione
4-Nitroisobenzofuran-1,3-dione, also known as a nitro-derivative of isobenzofuran, holds a notable place in organic chemistry. This compound belongs to a class of molecules characterized by their unique structural and electronic properties. Here are some fascinating insights:
- Reactivity: The presence of the nitro group (-NO2) significantly influences the reactivity of the compound. It acts as a powerful electron-withdrawing group, making the compound highly electrophilic and enhancing its potential in various chemical reactions.
- Applications: Compounds like 4-nitroisobenzofuran-1,3-dione are often explored for their potential applications in the development of pharmaceuticals, agrochemicals, and materials science due to their unique properties.
- Synthetic Utility: This compound can serve as an important intermediate in organic synthesis. Its structure allows for various functionalization pathways, making it valuable for researchers looking to create complex organic molecules.
- Nitro Compounds in Research: Nitro compounds are of great interest in material science and medicinal chemistry. Research has shown that they can exhibit interesting photophysical properties, which may lead to innovative applications in drug design and photodynamic therapy.
As chemists continue to explore the depths of organic compounds, 4-nitroisobenzofuran-1,3-dione stands out as a fascinating subject for study. Researchers delve into its properties not just for academic pursuit, but also to unlock new technologies and materials that could have profound implications in various industries.
Synonyms
3-Nitrophthalic anhydride
641-70-3
4-Nitro-2-benzofuran-1,3-dione
Phthalic anhydride, 3-nitro-
1,3-Isobenzofurandione, 4-nitro-
X2BXS9KCY2
NSC 4134
NSC-4134
EINECS 211-373-6
NSC 27006
NSC-27006
AI3-03720
DTXSID0060939
4-NITRO-1,3-ISOBENZOFURANDIONE
Phthalic anhydride, 3nitro
1,3Isobenzofurandione, 4nitro
DTXCID7044213
Phthalic anhydride, 3nitro (8CI)
Phthalic anhydride, 3-nitro-(8CI)
211-373-6
inchi=1/c8h3no5/c10-7-4-2-1-3-5(9(12)13)6(4)8(11)14-7/h1-3
rofzmkdrovblny-uhfffaoysa-n
4-nitroisobenzofuran-1,3-dione
MFCD00005921
4-nitro-isobenzofuran-1,3-dione
3-Nitrophthalicanhydride
3-nitro phthalic anhydride
nitrophthalic anhydride
UNII-X2BXS9KCY2
3-nitro-phtalic anhydride
SCHEMBL77252
3-nitrophtalic acid anhydride
3-nitrophthalic acid anhydride
CHEMBL2057876
3-Nitrophthalic anhydride, 98%
NSC4134
BCP27436
NSC27006
BBL019776
STL252564
4-Nitro-2-benzofuran-1,3-dione #
AKOS000121026
CS-W008730
FN26343
AC-23557
AS-10996
SY013547
DB-025351
N0245
NS00022614
EN300-18373
4-nitro-1,3-dihydro-2-benzofuran-1,3-dione
F11267
3-Nitrophthalic anhydride, purum, >=96.0% (NT)
Z57127499
F0001-1738
Solubility of 4-nitroisobenzofuran-1,3-dione
The solubility of 4-nitroisobenzofuran-1,3-dione is a key aspect to consider when discussing its chemical behavior and potential applications. This compound exhibits variable solubility depending on the solvent used. Generally, it shows:
When examining the factors affecting solubility, it's important to note the following:
One can summarize the solubility profile by noting that while 4-nitroisobenzofuran-1,3-dione can dissolve in both polar and nonpolar environments, its efficiency lies with organic solvents, where it finds greater solubility. This solubility behavior is crucial for its utilization in various chemical synthesis and applications.