[L17146] CAS 16382-15-3 | Ethyl 5-methylindole-2-carboxylate, 98% | Alfa
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Brand: Alfa Aesar
16382-15-3 | C12H13NO2 | ethyl 5-methyl-1H-indole-2-carboxylate
Chemical Identifiers
CAS
16382-15-3
Molecular Weight (g/mol)
203.24
Synonym
ethyl 5-methyl-1H-indole-2-carboxylate
SMILES
CCOC(=O)C1=CC2=CC(C)=CC=C2N1
InChI Key
KMVFKXFOPNKHEM-UHFFFAOYSA-N
Molecular Formula
C12H13NO2
IUPAC Name
ethyl 5-methyl-1H-indole-2-carboxylate
Specifications
Melting Point (clear melt)
159-167?C
Appearance (Color)
White or cream to pale brown
Form
Powder
Assay (GC)
≥97.5%
설명
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
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.
GHS Hazard and Precautionary Statements
Hazard Statements:
Risk & Safety
경고:RUO – Research Use Only
CAS16382-15-3FORMULAC12H13NO2
| Pakage | 1g, 5g |
|---|---|
| brand | Alfa Aesar |
