ETHYL 5-METHYLINDOLE-2-CARBOXYLATE

ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
  • CAS No.:16382-15-3
Other grades of this product :
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Basic information
Product Name:ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
Synonyms:1-ethyl-5-methyl-2-indolecarboxylate;Nsc30928;Ethyl 5-Methylindole-2-carboxylate;Ethyl 5-methylindole-2-carboxylate 5-Methyl-1H-indole-2-carboxylic acid ethyl ester;Ethyl 5-methylindole-2-carboxylate 97%;ETHYL 5-METHYLINDOLE-2-CARBOXYLATE;ETHYL 5-METHYL-1H-INDOLE-2-CARBOXYLATE;2-CARBETHOXY-5-METHYLINDOLE
CAS:16382-15-3
MF:C12H13NO2
MW:203.24
EINECS:
Product Categories:Heterocyclic Building Blocks;Indoles;Indoles and derivatives;Indole;Building Blocks
Mol File:16382-15-3.mol
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Chemical Properties
Melting point 162-164°C
Boiling point 236°C 4mm
density 1.177±0.06 g/cm3(Predicted)
Fp 236°C/4mm
storage temp. Sealed in dry,Room Temperature
pka15.19±0.30(Predicted)
Water Solubility Soluble in methanol, and dichloromethane. Insoluble in water.
BRN 159437
CAS DataBase Reference16382-15-3(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
HS Code 2933998090
MSDS Information
ProviderLanguage
ALFA English
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Usage And Synthesis
UsesReactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions 1 Reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists 2 Reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents 3 Reactant for Friedel-Crafts acylation with nitrobenzoyl chloride 4 Reactant for oximation reactions 5
UsesReactant 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
General DescriptionEthyl 5-methylindole-2-carboxylate (5-Methylindole-2-carboxylic acid ethyl ester) is an indole derivative. 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.
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Preparation Products And Raw materials

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