5-Methoxy-2-methylindol Produkt Beschreibung

5-METHOXY-2-METHYLINDOLE Struktur
1076-74-0
  • CAS-Nr.1076-74-0
  • Bezeichnung:5-Methoxy-2-methylindol
  • Englisch Name:5-METHOXY-2-METHYLINDOLE
  • Synonyma:5-Methoxy-2-methylindol
    NSC 63817;AKOS JY2082626;5-Methoxy-2-methyindole;2-Methyl-5-Methoxyindole;5-METHOXY-2-METHYLINDOLE;Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole 99%;1H-Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole, 99+%;5-Methoxy-2-Methylindole, 99+% 5GR
  • CBNumber:CB8174569
  • Summenformel:C10H11NO
  • Molgewicht:161.2
  • MOL-Datei:1076-74-0.mol
5-Methoxy-2-methylindol physikalisch-chemischer Eigenschaften
  • Schmelzpunkt: :86-88 °C(lit.)
  • Siedepunkt: :145 °C / 1.5mmHg
  • Dichte :1.0840 (rough estimate)
  • Brechungsindex :1.5200 (estimate)
  • storage temp.  : 0-6°C
  • Löslichkeit :Soluble in methanol (very faint turbidity.)
  • Aggregatzustand :Crystalline Powder or Crystals
  • Farbe :White to light beige
  • InChIKey :VSWGLJOQFUMFOQ-UHFFFAOYSA-N
  • CAS Datenbank :1076-74-0(CAS DataBase Reference)
Sicherheit
  • Kennzeichnung gefährlicher :Xi
  • R-Sätze: :36/37/38
  • S-Sätze: :37/39-26
  • WGK Germany  :3
  • HazardClass  :IRRITANT
  • HS Code  :29339900

5-METHOXY-2-METHYLINDOLE Chemische Eigenschaften,Einsatz,Produktion Methoden

  • R-Sätze Betriebsanweisung: R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
  • S-Sätze Betriebsanweisung: S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
    S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
  • Beschreibung 5-methoxy-2-methylindole is a useful organic raw material. It can be used as the reactant in the preparation of indolylquinoxalines by condensation reactions, in preparation of alkylindoles via Ir-catalyzed reductive alkylation, in arylation reactions in the presence of a palladium acetate catalyst, in enantioselective Friedel-Crafts alkylation, as well as in stereo selective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. It is also employed in inhibiting the chlorinating activity of myeloperoxidase (MPO) and in the metabolic synthesis of acrylacetic acid anti-inflammatory synthesis.
  • Chemische Eigenschaften white to light beige crystalline powder or
  • Verwenden An indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid antiinflammatory synthesis.
  • Verwenden reactant in preparation of indolylquinoxalines by condensation reactions1reactant in preparation of alkylindoles via Ir-catalyzed reductive alkylation2reactant in arylation reactions using a palladium acetate catalyst3reactant in enantioselective Friedel-Crafts alkylation4reactant in stereoselective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation5
  • Einzelnachweise https://www.alfa.com/en/catalog/B21348/
    http://www.sigmaaldrich.com/catalog/product/aldrich/m15451?lang=en&region=US
    https://pubchem.ncbi.nlm.nih.gov/compound/5-Methoxy-2-methylindole#section=2D-Structure
5-METHOXY-2-METHYLINDOLE Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
5-Methoxy-2-methylindol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
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1076-74-0, 5-METHOXY-2-METHYLINDOLE Verwandte Suche:
  • 5-METHOXY-2-METHYLINDOLE
  • AKOS JY2082626
  • 5-Methoxy-2-methylindole, 99+%
  • 5-Methoxy-2-methyindole
  • 5-Methoxy-2-Methylindole, 99+% 25GR
  • 5-Methoxy-2-Methylindole, 99+% 5GR
  • 2-Methyl-5-Methoxyindole
  • NSC 63817
  • 5-Methoxy-2-methylindole 99%
  • 1H-Indole, 5-methoxy-2-methyl-
  • Indole, 5-methoxy-2-methyl-
  • 1076-74-0
  • Simple Indoles
  • Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • -
  • Indoles and derivatives
  • Indole
  • Indoles
  • Simple Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Aromatics
  • Heterocycles
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Building Blocks
  • C10
  • Chemical Synthesis
  • Heterocyclic Building Blocks