| Identification | More | [Name]
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE | [CAS]
16382-15-3 | [Synonyms]
2-CARBETHOXY-5-METHYLINDOLE
2-CARBOXY-5-METHYLINDOLE
5-METHYL-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
5-METHYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
ETHYL 5-METHYL-1H-INDOLE-2-CARBOXYLATE
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
5-Methyl-2-indolecarboxylic acid ethyl ester
5-Me-ICA-OEt | [Molecular Formula]
C12H13NO2 | [MDL Number]
MFCD00022703 | [Molecular Weight]
203.24 | [MOL File]
16382-15-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
162-164°C | [Boiling point ]
236°C 4mm | [density ]
1.177±0.06 g/cm3(Predicted) | [Fp ]
236°C/4mm | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
15.19±0.30(Predicted) | [Water Solubility ]
Soluble in methanol, and dichloromethane. Insoluble in water. | [BRN ]
159437 | [CAS DataBase Reference]
16382-15-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3 |
| Hazard Information | Back Directory | [Uses]
Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions 1 Reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists 2 Reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents 3 Reactant for Friedel-Crafts acylation with nitrobenzoyl chloride 4 Reactant for oximation reactions 5 | [Uses]
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 | [General Description]
Ethyl 5-methylindole-2-carboxylate (5-Methylindole-2-carboxylic acid ethyl ester) is an indole derivative. 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. |
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