663190
Ethyl 5-methylindole-2-carboxylate
97%
Synonym(s):
5-Methylindole-2-carboxylic acid ethyl ester, NSC 30928
About This Item
Recommended Products
Assay
97%
form
solid
mp
160-164 °C
functional group
ester
SMILES string
CCOC(=O)c1cc2cc(C)ccc2[nH]1
InChI
1S/C12H13NO2/c1-3-15-12(14)11-7-9-6-8(2)4-5-10(9)13-11/h4-7,13H,3H2,1-2H3
InChI key
KMVFKXFOPNKHEM-UHFFFAOYSA-N
General description
Application
- 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
- Reactant for oximation reactions
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
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