Thermo Scientific Chemicals

Ethyl 5-methylindole-2-carboxylate, 98%, Thermo Scientific Chemicals

Catalog number: L17146.06
5 g, Each
Thermo Scientific Chemicals

Ethyl 5-methylindole-2-carboxylate, 98%, Thermo Scientific Chemicals

Catalog number: L17146.06
5 g, Each
Quantity
Catalog number: L17146.06
also known as L17146-06
Price (USD)
Quantity
-

Chemical Identifiers

CAS
16382-15-3
IUPAC Name
ethyl 5-methyl-1H-indole-2-carboxylate
Molecular Formula
C12H13NO2
InChI Key
KMVFKXFOPNKHEM-UHFFFAOYSA-N
SMILES
CCOC(=O)C1=CC2=CC(C)=CC=C2N1
Melting Point (clear melt)
159-167?C
Appearance (Color)
White or cream to pale brown
Form
Powder
Assay (GC)
≥97.5%

Description

Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions, reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists, reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents, reactant for Friedel-Crafts acylation with nitrobenzoyl chloride. Indole ring system is an important building block or intermediate in the synthesis of many pharmaceutical agents. It is formed during the Fischer indolization of ethyl pyruvate 2-[2-(methanesulfonyloxy)-4-methyl]phenylhydrazine.
  • Reactant for oximation reactions

    This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

    Applications
    Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions, reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists, reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents, reactant for Friedel-Crafts acylation with nitrobenzoyl chloride. Indole ring system is an important building block or intermediate in the synthesis of many pharmaceutical agents. It is formed during the Fischer indolization of ethyl pyruvate 2-[2-(methanesulfonyloxy)-4-methyl]phenylhydrazine. · Reactant for oximation reactions

    Solubility
    Soluble in methanol, and dichloromethane. Insoluble in water.

    Notes
    Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
    RUO – Research Use Only

    Figures

    Documents & Downloads

    Certificates

      Frequently asked questions (FAQs)

      Citations & References

      Search citations by name, author, journal title or abstract text