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Potassium phthalimide

Potassium phthalimide structure

Potassium phthalimide 

structure
  • CAS No:

    1074-82-4

  • Formula:

    C8H5NO2.K

  • Chemical Name:

    Potassium phthalimide

  • Synonyms:

    1H-Isoindole-1,3(2H)-dione,potassium salt (1:1);Phthalimide,potassium salt;1H-Isoindole-1,3(2H)-dione,potassium salt;Potassium,phthalimido-;Phthalimide,potassium deriv.;Potassium phthalimide;N-Potassiophthalimide;Potassium phthalimidate;Phthalimidopotassium;Phthalimide potassium;Potassium isoindoline-1,3-dione;Isoindole-1,3-dione potassium salt;Potassium 2,3-dihydro-1H-isoindole-1,3-dione;Potassium 1,3-dioxoisoindolin-2-ide;1H-Isoindole-1,3(2H)-dione,potassium salt,ion(1-) (1:1);92014-68-1;1239707-97-1;1445950-63-9;1687743-72-1;1962933-27-2;2454020-25-6

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

slight yellow-green to white powder

Potassium phthalimide Basic Attributes

185.22

184.988

3598719

214-046-6

X6KKA27DIL

DTXSID5027358

29251995

Characteristics

35.1

0.68480

White to yellow or greenish Crystalline Powder

1.63

>250 °C

366C

170.9ºC

water: soluble 50mg/mL, clear to slightly hazy, colorless to yellow

Store at RT.

Safety Information

3

36/37/38

22-24/25-26-60-37

Xi

Stable at room temperature in closed containers under normal storage and handling conditions.

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 71 companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

phthalimide

Potassium phthalimide Use and Manufacturing

Uses

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.

1H-Isoindole-1,3(2H)-dione, potassium salt (1:1): ACTIVE|SOME 35 SUBSTANCES AND THEIR HALO AND NITRO DERIVATIVES (INCLUDING POTASSIUM PHTHALIMIDE) ARE DESCRIBED AS ANTIDOTES TO HERBICIDES. N-HYDROXYPHTHALIMIDE TOTALLY PROTECTED WINTER WHEAT AGAINST PHYTOTOXICITY OF 2-CHLORO-4-ETHYL-(ETHYLAMINO)-6-CYANOPROPYLAMINO-S-TRIAZINE.

Computed Properties

Molecular Weight:185.22
Hydrogen Bond Acceptor Count:3
Exact Mass:184.98790986
Monoisotopic Mass:184.98790986
Topological Polar Surface Area:35.1
Heavy Atom Count:12
Complexity:195
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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