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

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

Catalog Number p-7047000
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Quantity:
1 g
5 g
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16382-15-3
C12H13NO2
203.241
MFCD00022703
KMVFKXFOPNKHEM-UHFFFAOYSA-N
ethyl 5-methylindole-2-carboxylate, 2-carbethoxy-5-methylindole, 5-methylindole-2-carboxylic acid ethyl ester, 5-methyl-1h-indole-2-carboxylic acid ethyl ester, pubchem7940, acmc-1brcs, 5-methyl-2-ethoxycarbonyl indole, ethyl 5-methyl-2-indolecarboxylate, 5-methyl-1h-indole-2-carboxylic acid, ethyl ester
232919
ethyl 5-methyl-1H-indole-2-carboxylate
CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C
This item is not returnable. View return policy
16382-15-3
C12H13NO2
203.241
MFCD00022703
KMVFKXFOPNKHEM-UHFFFAOYSA-N
ethyl 5-methylindole-2-carboxylate, 2-carbethoxy-5-methylindole, 5-methylindole-2-carboxylic acid ethyl ester, 5-methyl-1h-indole-2-carboxylic acid ethyl ester, pubchem7940, acmc-1brcs, 5-methyl-2-ethoxycarbonyl indole, ethyl 5-methyl-2-indolecarboxylate, 5-methyl-1h-indole-2-carboxylic acid, ethyl ester
232919
ethyl 5-methyl-1H-indole-2-carboxylate
CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C

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.
    TRUSTED_SUSTAINABILITY
    Melting Point 161°C to 165°C
    Boiling Point 236°C (4 mmHg)
    Quantity 1 g
    Beilstein 159437
    Solubility Information Soluble in methanol,and dichloromethane. Insoluble in water.
    Formula Weight 203.24
    Percent Purity 99%
    Chemical Name or Material Ethyl 5-methylindole-2-carboxylate

    RUO – Research Use Only

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