| Weight | 185.223 g/mol |
|---|---|
| Formula | C8H4KNO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1074-82-4 (1074-82-4)
phthalimide · potassium phthalimide · phthalimide potassium salt
Score:
#2355 in Physics
,
#7205 in Chemistry
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- Phthalimide-Based Polymers for High Performance Organic Thin-Film Transistors (Journal of the American Chemical Society, 2009)
- Direct Catalytic Trifluoromethylthiolation of Boronic Acids and Alkynes Employing Electrophilic ShelfStable N(trifluoromethylthio)phthalimide (Angewandte Chemie, 2014)
- An Improved Procedure for the Condensation of Potassium Phthalimide with Organic Halides (Journal of the American Chemical Society, 1950)
- Effect of Linking Bridge Modifications on the Antipsychotic Profile of Some Phthalimide and Isoindolinone Derivatives (Journal of Medicinal Chemistry, 1996)
- Phthalimide conjugation as a strategy for in vivo target protein degradation (Science, 2015)
- Potassium phthalimide-N-oxyl: a novel, efficient, and simple organocatalyst for the one-pot three-component synthesis of various 2-amino-4H-chromene derivatives in water (Tetrahedron, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phthalimide
- potassium phthalimide
- phthalimide potassium salt
- phthalimide calcium (2:1) salt
-
SMILESC1=CC=C2C(=C1)C(=O)[N-]C2=O.[K+]
-
InChIKeyFYRHIOVKTDQVFC-UHFFFAOYSA-M
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