CAS 1074-82-4
:Potassium phthalimide
Description:
Potassium phthalimide is an organic compound with the formula C8H4KNO2, characterized by its white crystalline appearance. It is the potassium salt of phthalimide and is commonly used in organic synthesis, particularly in the preparation of amines through the Gabriel synthesis. This compound is soluble in water and exhibits moderate stability under standard conditions. Potassium phthalimide acts as a nucleophile, making it valuable in various chemical reactions, including alkylation processes. Additionally, it has applications in the pharmaceutical industry and in the production of agrochemicals. The compound is generally considered to have low toxicity, but standard safety precautions should be observed when handling it, as with any chemical substance. Its reactivity and solubility properties make it a useful reagent in laboratory settings, contributing to its significance in synthetic organic chemistry.
Formula:C8H5NO2·K
InChI:InChI=1S/C8H5NO2.K/c10-7-5-3-1-2-4-6(5)8(11)9-7;/h1-4H,(H,9,10,11);
InChI key:InChIKey=BYXYCUABYHCYLY-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1)=CC=CC2.[K]
Synonyms:- 1H-Isoindole-1,3(2H)-dione, potassium salt (1:1)
- 1H-Isoindole-1,3(2H)-dione, potassium salt, ion(1-) (1:1)
- Isoindole-1,3-dione potassium salt
- N-Kaliumphthalimid
- N-Potassiophthalimide
- N-potassium phthalimide
- Phtalimide N-potassique
- Phthalimide potassium
- Phthalimide, potassium deriv.
- Phthalimide, potassium salt
- Phthalimidopotassium
- Potassium 1,3-dioxoisoindolin-2-ide
- Potassium 2,3-dihydro-1H-isoindole-1,3-dione
- Potassium isoindoline-1,3-dione
- Potassium phthalimidate
- Potassium phthalimide
- Potassium salt of phthalimide
- Potassium, phthalimido-
- ftalimida N-potasica
- See more synonyms
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Found 9 products.
Phthalimide Potassium Salt
CAS:Formula:C8H4KNO2Purity:>98.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:185.22Potassium phthalimide, 98+%
CAS:<p>Potassium phthalimide is used as an intermediate in the synthesis of N-alkylated phthalimides, which is involved in the preparation of primary amines (Gabriel synthesis) by the hydrolysis reaction. It is also used as an intermediate for synthetic indigo, pigments, dyes and pharmaceuticals. Further, </p>Formula:C8H4KNO2Purity:98+%Color and Shape:White to cream to yellow to green, Crystalline powder or powderMolecular weight:185.22Phthalimide potassium salt
CAS:<p>Phthalimide potassium salt</p>Formula:C8H4NO2·KPurity:97%Color and Shape: white powderMolecular weight:185.22g/molPotassium 1,3-dioxoisoindolin-2-ide
CAS:Formula:C8H4KNO2Purity:98.0%Color and Shape:SolidMolecular weight:185.223Potassium Phthalimide
CAS:Controlled Product<p>Applications Potassium Phthalimide is a green, solid-base organocatalys.<br>References Kiyani, H., Ghiasi, M.: Chinese Chem. Lett., 25, 313 (2014)<br></p>Formula:C8H4NO2·KColor and Shape:NeatMolecular weight:185.22Phthalimide potassium
CAS:<p>Phthalimide potassium is a chemical that reacts with oxygen nucleophiles to form the corresponding N-hydroxyphthalimide. It has been shown as an effective treatment for cancer by targeting tumor cells and inhibiting their growth. The mechanism of action involves binding to 5-HT2 receptors in the cell membrane, which leads to inhibition of the enzyme adenylate cyclase, leading to decreased levels of cAMP. This decreases the activity of protein kinase A, which in turn leads to decreased production of proteins such as p21WAF1/CIP1, which are required for cell cycle progression. Phthalimide potassium has also been shown to be active against HIV infection and may be useful for other diseases involving virus infections. This drug binds covalently with HLA proteins on the surface of infected cells and inhibits viral replication by preventing reverse transcription.</p>Formula:C8H4KNO2Color and Shape:White PowderMolecular weight:185.22 g/mol
