Phthalimide potassium salt - ≥98% , CAS No.1074-82-4

CAS: 1074-82-4 Cat. No.: P106220 Summenformel: C₈H₄KNO₂ Molekulargewicht: 185.22 Beilstein Registry Number: 3598719 EG-Nummer: 214-046-6

GRADE & PURITY ≥98%

Synonyms

Potassium 1,3-dioxoisoindolin-2-ide | DTXCID007358 | AKOS034830283 | AM90358 | 2-potassio-2,3-dihydro-1H-isoindole-1,3-dione | POTASSIUM PHTHALIMIDE | FT-0651552 | Q413572 | AKOS000121936 | BCP26871 | X6KKA27DIL | HSDB 5781 | potassium 1,3-dioxo-1,3-dihyd

Storage

Argon charged,Room temperature

Shipped In

Normal

Übersicht

A reagent which transforms allyl- and alkyl halides into protected primary amines.
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.

Application

Condensation of phthalimide potassium with organic halide in dimethylformamide has been reported.Reaction of potassium phthalimide and sulfur monochloride in petroleum ether has been studied.
Phthalimide potassium salt was employed as organocatalyst for the cyanosilylation of various carbonyl compounds under extremely mild conditions. It was also employed as reagent for the transformation of allyl- and alkyl halides into protected primary amines.

Specifications

Synonyme

Potassium 1,3-dioxoisoindolin-2-ide | DTXCID007358 | AKOS034830283 | AM90358 | 2-potassio-2,3-dihydro-1H-isoindole-1,3-dione | POTASSIUM PHTHALIMIDE | FT-0651552 | Q413572 | AKOS000121936 | BCP26871 | X6KKA27DIL | HSDB 5781 | potassium 1,3-dioxo-1,3-dihyd

Spezifikationen & Reinheit

≥98%

Storage

Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

504762543

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504762543

Kanonisches Lächeln

C1=CC=C2C(=C1)C(=O)[N-]C2=O.[K+]

IUPAC Name

potassium;isoindol-2-ide-1,3-dione

InChIKey

FYRHIOVKTDQVFC-UHFFFAOYSA-M

INCHI

1S/C8H5NO2.K/c10-7-5-3-1-2-4-6(5)8(11)9-7;/h1-4H,(H,9,10,11);/q;+1/p-1

Isomere SMILES

C1=CC=C2C(=C1)C(=O)[N-]C2=O.[K+]

WGK Deutschland

3

Molekulargewicht

185.22

Beilstein

3598719

Reaxy-Rn

473209

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=473209&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Isoindoles and derivatives
      • Subclass Isoindolines
        • Ebene5 Isoindolones
          • Ebene6 Phthalimides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Isoindoles and derivatives
• Subclass: Isoindolines
• Intermediate Tree Nodes: Isoindolones
• Direct Parent: Phthalimides
• Alternative Parents: Isoindoles Benzenoids Carboxylic acids and derivatives Carbene-type 1,3-dipolar compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic potassium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phthalimide - Isoindole - Benzenoid - Carboxylic acid derivative - Carbene-type 1,3-dipolar compound - Organic 1,3-dipolar compound - Azacycle - Organic alkali metal salt - Organic nitrogen compound - Organic potassium salt - Organic salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BCHE Tclin Butyrylcholinesterase (7174 Activities)

Discover Target: BCHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water
• Empfindlichkeit: Moisture Sensitive
• Schmelzpunkt (°C): >300°C
• Molekulargewicht: 185.220 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 184.988 Da
• Monoisotopic Mass: 184.988 Da
• Topological Polar Surface Area: 35.100 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 195.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Häufig gestellte Fragen

What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 1074-82-4, the molecular formula is C8H4KNO2, and the molecular weight is 185.22 g/mol. InChIKey FYRHIOVKTDQVFC-UHFFFAOYSA-M.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.