ETHYL 5-METHYLINDOLE-2-CARBOXYLATE

ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Structure
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

ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Properties

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
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
1
0 0

ETHYL 5-METHYLINDOLE-2-CARBOXYLATE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 663190 Ethyl 5-methylindole-2-carboxylate 97% 16382-15-3 1G ₹4200.1 2022-06-14 Buy
Sigma-Aldrich(India) 663190 Ethyl 5-methylindole-2-carboxylate 97% 16382-15-3 5G ₹11939.98 2022-06-14 Buy
Product number Packaging Price Buy
663190 1G ₹4200.1 Buy
663190 5G ₹11939.98 Buy

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

Global( 149)Suppliers
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CHEMAZON LABORATORIES +91 9848551964 Hyderabad, India 1320 58 Inquiry
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Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30253 58 Inquiry

ETHYL 5-METHYLINDOLE-2-CARBOXYLATE Spectrum

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