Sale di potassio di ftalimmide - ≥98% , CAS No.1074-82-4

CAS: 1074-82-4 Cat. No.: P106220 Formula: C₈H₄KNO₂ Peso molecolare: 185.22 Beilstein Registry Number: 3598719 Numero EC: 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

Normale

Panoramica

Reagente che trasforma allil- e alogenuri alchilici in ammine primarie protette.
Viene solitamente utilizzato come organocatalizzatore per la cianosilazione di vari composti carbonilici in condizioni estremamente blande, nonché come reagente per la trasformazione di allil- e alogenuri alchilici in ammine primarie protette.

Specifications

Sinonimi

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

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normale

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

504762543

Pubchem Sid Url

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

Sorrisi canonici

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

Isomeri SMILES

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

WGK Germania

3

Peso molecolare

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
    • Classe Isoindoles and derivatives
      • Subclass Isoindolines
        • Level5 Isoindolones
          • Level6 Phthalimides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: 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
• Descrizione: 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

Obiettivi associati (umani)

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water
• Sensibilità: Moisture Sensitive
• Punto di fusione (°C): >300°C
• Peso molecolare: 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

Domande frequenti

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.