CAS 3485-84-5: Vinylphthalimide
Formula:C10H7NO2
InChI:InChI=1S/C10H7NO2/c1-2-11-9(12)7-5-3-4-6-8(7)10(11)13/h2-6H,1H2
InChI key:InChIKey=IGDLZDCWMRPMGL-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1C=C)=CC=CC2
Synonyms:- 1H-Isoindole-1,3(2H)-dione, 2-ethenyl-
- 2-Ethenyl-1H-isoindole-1,3(2H)-dione
- 2-Ethenyl-2,3-dihydro-1H-isoindole-1,3-dione
- 2-Ethenylisoindole-1,3-dione
- 2-Vinyl-1H-isoindole-1,3(2H)-dione
- 2-Vinylisoindoline-1,3-dione
- N-Vinylphthalamide
- Nsc 10395
- Phthalimide, N-vinyl-
- Vinylphthalimide
- N-Vinylphthalimide
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Found 7 products.
N-Vinylphthalimide, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Purity:99%Color and Shape:Off-white to light yellow, Crystalline powderN-Vinylphthalimide, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C10H7NO2Purity:99%Color and Shape:Crystals or powder or crystalline powder, White to cream to pale yellowMolecular weight:173.172-Vinyl-1H-isoindole-1,3(2H)-dione
CAS:Purity:97.00%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:173.17100524902344N-Vinylphthalimide
CAS:Formula:C10H7NO2Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:173.17N-Vinylphthalimide
CAS:N-Vinylphthalimide is the monomer for a polyvinylpyrrolidone synthesis that can be used to create polymer films. It is also a reactive compound, which reacts with palladium complexes in the presence of ethyl diazoacetate to form vinylpyrrolidone. N-Vinylphthalimide has significant antifungal activity and can be used as an alternative to amphotericin B. This compound was synthesized by reacting hydrogen chloride with sodium hydrogen sulfate in the presence of fatty acids. The reaction mechanism involves acylation, followed by hydrolysis of the ester product and hydrogenation of the resultant carboxylic acid. N-Vinylphthalimide's antifungal activity has been shown using a turbidimetric method that detects changes in light scattering induced by fungal growth.Formula:C10H7NO2Purity:Min. 95%Molecular weight:173.17 g/mol2-Vinylisoindoline-1,3-dione
CAS:Formula:C10H7NO2Purity:98%Color and Shape:SolidMolecular weight:173.1681
