ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
- CAS No.
- 16382-15-3
- Chemical Name:
- ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
- Synonyms
- Nsc30928;5-Me-ICA-OEt;2-CARBOXY-5-METHYLINDOLE;2-CARBETHOXY-5-METHYLINDOLE;ETHYL 5-METHYLINDOLE-2-CARBOXYLATE;Ethyl-5-methyl-inodole-2-carboxylate;1-ethyl-5-methyl-2-indolecarboxylate;Ethyl 5-methylindole-2-carboxylate 97%;ETHYL 5-METHYL-1H-INDOLE-2-CARBOXYLATE;5-METHYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
- CBNumber:
- CB4383136
- Molecular Formula:
- C12H13NO2
- Molecular Weight:
- 203.24
- MOL File:
- 16382-15-3.mol
- MSDS File:
- SDS
- Modify Date:
- 2023/4/23 13:52:06
Melting point | 162-164°C |
---|---|
Boiling point | 236°C 4mm |
Density | 1.177±0.06 g/cm3(Predicted) |
Flash point | 236°C/4mm |
storage temp. | Sealed in dry,Room Temperature |
pka | 15.19±0.30(Predicted) |
form | crystalline powder |
color | Light yellow to beige |
Water Solubility | Soluble in methanol, and dichloromethane. Insoluble in water. |
BRN | 159437 |
CAS DataBase Reference | 16382-15-3(CAS DataBase Reference) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
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Signal word | Warning | |||||||||
Hazard statements | H315-H319-H335 | |||||||||
Precautionary statements | P280-P305-P351 | |||||||||
Safety Statements | 22-24/25 | |||||||||
WGK Germany | 3 | |||||||||
HS Code | 2933998090 | |||||||||
NFPA 704 |
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ETHYL 5-METHYLINDOLE-2-CARBOXYLATE price More Price(2)
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Chemical Properties,Uses,Production
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
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.
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Preparation Products And Raw materials
Raw materials
Preparation Products
Global( 149)Suppliers
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
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CHEMAZON LABORATORIES | +91 9848551964 | Hyderabad, India | 1320 | 58 | Inquiry |
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16382-15-3(ETHYL 5-METHYLINDOLE-2-CARBOXYLATE)Related Search:
Ethyl 5-cyanoindole-2-carboxylate
5-TERT-BUTYL-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
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5-ETHOXYCARBONYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
Ethyl indole-2-carboxylate
Methyl indole-2-carboxylate
5-Methylindole
5-METHYLINDOLE-2-CARBOXYLIC ACID
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Nsc30928
Ethyl 5-Methylindole-2-carboxylate
Ethyl 5-methylindole-2-carboxylate
5-Methyl-1H-indole-2-carboxylic acid ethyl ester
Ethyl 5-methylindole-2-carboxylate 97%
ETHYL 5-METHYLINDOLE-2-CARBOXYLATE
ETHYL 5-METHYL-1H-INDOLE-2-CARBOXYLATE
2-CARBETHOXY-5-METHYLINDOLE
2-CARBOXY-5-METHYLINDOLE
5-METHYL-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
5-METHYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
5-Me-ICA-OEt
5-Methyl-2-indolecarboxylic acid ethyl ester
1H-Indole-2-carboxylic acid, 5-methyl-, ethyl ester
Ethyl-5-methyl-inodole-2-carboxylate
1-ethyl-5-methyl-2-indolecarboxylate
1H-Indole-2-carboxylic acid, 5-methyl-, ethyl ester (9CI, ACI)
5-methyl-1H-Indole-2-carboxylic acid ethyl ester (9CI ACI)
16382-15-3
Building Blocks
Heterocyclic Building Blocks
Indoles
Heterocyclic Building Blocks
Indoles
Building Blocks
Indoles and derivatives
Indole