missing translation for 'onlineSavingsMsg'
Learn More

Ethyl 5-methylindole-2-carboxylate, 98%

Catalog No. AAL1714603
Change view
Click to view available options
Quantity:
1 g
5 g
2 product options available for selection
Product selection table with 2 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
AAL1714603 1 g
AAL1714606 5 g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 2 options available.
2 options
Catalog No. AAL1714603 Supplier Thermo Scientific Chemicals Supplier No. L1714603
Only null left

CAS: 16382-15-3 | C12H13NO2 | 203.241 g/mol

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.

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, 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

Specifications

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
TSCA No
Recommended Storage Ambient temperatures

RUO – Research Use Only