Identification | More | [Name]
Potassium phthalimide | [CAS]
1074-82-4 | [Synonyms]
n-potassium phthalimide PHTHALIMIDE POTASSIUM PHTHALIMIDE, POTASSIUM DERIVATIVE PHTHALIMIDE POTASSIUM SALT POTASSIUM PHTHALAMIDE POTASSIUM PHTHALIMIDE 1H-Isoindole-1,3(2H)-dione,potassiumsalt n-potassiophthalimide potassiumphthalimidate PotassiumPhthalylimide99% Potassium phtalimide, 97% Phthlimide 1,3-dihydro-1,3-dioxoisoindole potassium salt PHTHALYLIMIDE POTASSIUM SALT Potassium phthalimide, 98+% 1,3-Dihydro-1,3-dioxoisoindole potassium salt, Potassium phthalimide Phthalimidopotassium Potassium isoindol-2-ide-1,3-dione Potassium phthalimide ,99% 1,3-Dioxo-1,3-dihydro-2H-isoindole-2-ylpotassium | [EINECS(EC#)]
214-046-6 | [Molecular Formula]
C8H4KNO2 | [MDL Number]
MFCD00005887 | [Molecular Weight]
185.22 | [MOL File]
1074-82-4.mol |
Chemical Properties | Back Directory | [Appearance]
slight yellow-green to white powder | [Melting point ]
>300°C
| [Boiling point ]
366C | [density ]
1.63 | [storage temp. ]
Store at RT. | [solubility ]
water: soluble50mg/mL, clear to slightly hazy, colorless to yellow | [form ]
Crystalline Powder | [color ]
White to yellow or greenish | [PH]
pH (50g/l, 25℃) : 10.5~12.5 | [Water Solubility ]
Soluble in water. | [Sensitive ]
Moisture Sensitive | [Detection Methods]
T,NMR | [BRN ]
3598719 | [CAS DataBase Reference]
1074-82-4(CAS DataBase Reference) | [Storage Precautions]
Moisture sensitive | [EPA Substance Registry System]
1074-82-4(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29251995 | [Hazardous Substances Data]
1074-82-4(Hazardous Substances Data) |
Raw materials And Preparation Products | Back Directory | [Preparation Products]
3-N-Boc-amino-azetidine-->5-(AMINOMETHYL)-1-METHYLPYRROLIDIN-2-ONE-->1-Boc-3-(Amino)azetidine-->2-Phenoxyethylamine-->1-(1-METHYL-1H-PYRAZOL-3-YL)METHANAMINE-->2-(AMINOMETHYL)CYCLOPROPANECARBOXYLIC ACID-->N,N-Dimethylethylenediamine-->(2-Aminoethyl)phosphonic acid-->4-(4-CHLOROPHENYL)-1,2,3-THIADIAZOL-5-AMINE-->4-PYRROLIDINOBUTYLAMINE-->4-PHENYL-1,2,3-THIADIAZOL-5-AMINE-->Tetrakis(decyl)ammonium bromide-->3-Amino-5-methylisoxazole-->DIMETHYL POPOP-->N,N,N'-TRIMETHYL-1,3-PROPANEDIAMINE-->4-Amino-1-butanol-->4-[4-(TRIFLUOROMETHYL)PHENYL]-1,2,3-THIADIAZOL-5-AMINE-->4-(4-METHOXYPHENYL)-1,2,3-THIADIAZOL-5-AMINE-->TRIDODECYLAMINE-->4-CHLORO-2-METHYLBENZYLAMINE-->TERT-BUTYL 4-(AMINOMETHYL)PYRIDIN-2-YLCARBAMATE-->6-(TERT-BUTOXYCARBONYLAMINO-METHYL)-PYRIDINE-2-CARBOXYLIC ACID-->3-Bromopropylamine hydrobromide-->(2-TERT-BUTOXYFORMAMIDO-PYRIDIN-4-YL)METHYL METHANESULFONATE-->1-(3-Aminopropyl)piperidine-->6-(AMINOMETHYL)-2-PYRIDINE CARBOXYLIC ACID-->3-[(Benzyloxycarbonyl)amino]propionaldehyde-->2,2'-OXYBIS(ETHYLAMINE) HYDROCHLORIDE-->3-(3,5-DIMETHYL-PYRAZOL-1-YL)-PROPYLAMINE-->6-(AMINOMETHYL)PYRIDINE-2-CARBOHYDRAZIDE-->2-(3-BROMO-1-METHYL-2-OXOPROPYL)-L H-ISINDOLE-1,3-(2H)-DIONE-->3-NITROBENZYLAMINE-->2-(1-Methyl-2-oxopropyl)-1H-isoindole-1,3-(2H)-dione |
Hazard Information | Back Directory | [Chemical Properties]
slight yellow-green to white powder | [Uses]
Potassium phthalimide is usually used as organocatalyst for the cyanosilylation of various carbonyl compounds under extremely mild conditions,and also used as reagent for the transformation of allyl- and alkyl halides into protected primary amines.
| [Purification Methods]
The solid may contain phthalimide and K2CO3 from hydrolysis. If too much hydrolysis has occurred (this can be checked by extraction with cold Me2CO in which the salt is insoluble, evaporate the Me2CO and weigh the residue), it would be better to prepare it afresh. If little hydrolysis has occurred, then recrystallise it from a large volume of EtOH, and wash the solid with a little Me2CO and dry it in a continuous vacuum to constant weight. [Salzerg & Supriawski Org Synth Coll Vol I 119 1941, Raman & IR: Hase J Mol Struct 48 33 1978, Dykman Chem Ind (London) 40 1972, IR, NMR: Assef et al. Bull Soc Chim Fr II 167 1979, Beilstein 21/10 V 270.] |
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