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Alfa Aesar™ Ethyl 5-methylindole-2-carboxylate, 99%

$49.66 - $164.55

Chemical Identifiers

CAS 16382-15-3
Molecular Formula C12H13NO2
Formula Weight 203.24
MDL Number MFCD00022703
Beilstein 159437
Synonym 5-Methylindole-2-carboxylic acid ethyl ester
Chemical Name or Material Ethyl 5-methylindole-2-carboxylate
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Products ${productFamilyLength}
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAL1714603 SDS Alfa Aesar™
L1714603
1g Each for $49.66
AAL1714606 SDS Alfa Aesar™
L1714606
5g Each for $164.55
Specifications

Description

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.
Description & Specifications

Chemical Identifiers

16382-15-3
203.24
159437
Ethyl 5-methylindole-2-carboxylate
C12H13NO2
MFCD00022703
5-Methylindole-2-carboxylic acid ethyl ester

Specifications

16382-15-3
203.24
159437
236°C (4mmHg)
1g
99%
C12H13NO2
MFCD00022703
5-Methylindole-2-carboxylic acid ethyl ester
161° to 165°C
Ethyl 5-methylindole-2-carboxylate