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

$48.43 - $158.84

Chemical Identifiers

CAS 16382-15-3
Molecular Formula C12H13NO2
Molecular Weight (g/mol) 203.241
MDL Number MFCD00022703
InChI Key KMVFKXFOPNKHEM-UHFFFAOYSA-N
Synonym 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, ethyl 5-methylindole-2-carboxylate, 5-methyl-1h-indole-2-carboxylic acid, ethyl ester
PubChem CID 232919
IUPAC Name ethyl 5-methyl-1H-indole-2-carboxylate
SMILES CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C
View More Specs

Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAL1714603 View Documents Alfa Aesar™
L1714603
1g Each for $48.43
 
AAL1714606 View Documents Alfa Aesar™
L1714606
5g Each for $158.84
 
Description

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.
Specifications

Chemical Identifiers

16382-15-3
203.241
KMVFKXFOPNKHEM-UHFFFAOYSA-N
232919
CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C
C12H13NO2
MFCD00022703
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, ethyl 5-methylindole-2-carboxylate, 5-methyl-1h-indole-2-carboxylic acid, ethyl ester
ethyl 5-methyl-1H-indole-2-carboxylate

Specifications

236°C (4mmHg)
1g
C12H13NO2
159437
KMVFKXFOPNKHEM-UHFFFAOYSA-N
ethyl 5-methyl-1H-indole-2-carboxylate
232919
99%
161°C to 165°C
16382-15-3
MFCD00022703
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, ethyl 5-methylindole-2-carboxylate, 5-methyl-1h-indole-2-carboxylic acid, ethyl ester
CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C
203.241
203.24
Ethyl 5-methylindole-2-carboxylate