CAS 89-40-7
:4-Nitrophthalimide
Description:
4-Nitrophthalimide is an organic compound characterized by its structure, which consists of a phthalimide core substituted with a nitro group at the 4-position. It appears as a yellow crystalline solid and is known for its relatively high melting point. This compound is primarily used in organic synthesis and as a precursor for various chemical reactions, including the preparation of dyes and pharmaceuticals. 4-Nitrophthalimide exhibits moderate solubility in organic solvents such as acetone and ethanol, but is less soluble in water. Its chemical properties include the ability to undergo nucleophilic substitution reactions, making it a valuable intermediate in the synthesis of more complex molecules. Additionally, it can act as a photoinitiator in polymerization processes due to its ability to absorb UV light. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective equipment should be used to minimize exposure.
Formula:C8H4N2O4
InChI:InChI=1S/C8H4N2O4/c11-7-5-2-1-4(10(13)14)3-6(5)8(12)9-7/h1-3H,(H,9,11,12)
InChI key:InChIKey=ANYWGXDASKQYAD-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1)=CC=C(N(=O)=O)C2
Synonyms:- 1H-Isoindole-1,3(2H)-dione, 5-nitro-
- 4-Nitro Phthalimide
- 4-Nitro-1,2-Benzene Dicarboxylic Acid, Imide
- 5-Nitro-1,3-Dihydro-2H-Isoindol-1,3-Dione
- 5-Nitro-1H-Isoindole-1,3(2H)-Dione
- 5-Nitroisoindole-1,3-Dione
- 5-Nitroisoindoline-1,3-Dione
- 5-Nitrophthalimide
- Akos B028733
- NSC 5394
- Phthalimide, 4-nitro-
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
4-Nitrophthalimide
CAS:Formula:C8H4N2O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:192.135-Nitroisoindoline-1,3-dione
CAS:Formula:C8H4N2O4Purity:95%Color and Shape:SolidMolecular weight:192.12844-Nitrophthalimide
CAS:<p>4-Nitrophthalimide is a nitroimidazole compound that has been shown to be active against bacterial strains belonging to the group P2. It is also soluble in organic solvents such as chloroform, ethanol, and acetone. 4-Nitrophthalimide has been used for experimental solubility data and as a pharmaceutical preparation. The reaction of 4-nitrophthalimide with diazonium salt produces 3-nitrophthalic anhydride, which is then hydrolyzed by hydrochloric acid to form nitrobenzene. This reaction can be monitored using fluorescence resonance spectroscopy.</p>Formula:C8H4N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:192.13 g/mol5-Nitroisoindoline-1,3-dione
CAS:Formula:C8H4N2O4Purity:95%Color and Shape:Solid, White to yellow powderMolecular weight:192.13





