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ETHYL 2-METHYL-3-INDOLEACETATE

CAS No.
21909-49-9
Chemical Name:
ETHYL 2-METHYL-3-INDOLEACETATE
Synonyms
Nsc289352;Ethyl 2-methylindoleacetate;ETHYL 2-METHYL-3-INDOLEACETATE;Ethyl 2-methyl-3-indoleacetate 98%;Ethyl 2-Methyl-1H-indole-3-acetate;ethyl 2-(2-methyl-1H-indol-3-yl)acetate;2-(2-methyl-2-indolyl)acetic acid ethyl ester;1H-Indole-3-acetic acid, 2-Methyl-, ethyl ester
CBNumber:
CB8718497
Molecular Formula:
C13H15NO2
Molecular Weight:
217.26
MDL Number:
MFCD02093647
MOL File:
21909-49-9.mol
MSDS File:
SDS
Last updated:2023-06-29 08:28:15

ETHYL 2-METHYL-3-INDOLEACETATE Properties

Melting point 95 °C(Solv: ethyl ether (60-29-7))
Boiling point 195-196 °C/3.5 mmHg (lit.)
Density 1.11 g/mL at 25 °C (lit.)
refractive index n20/D 1.571(lit.)
Flash point >230 °F
pka 17.27±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3

ETHYL 2-METHYL-3-INDOLEACETATE price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 511161 Ethyl 2-methyl-3-indoleacetate 98% 21909-49-9 5g $166 2023-06-20 Buy
TRC E940635 Ethyl 2-methyl-3-indoleacetate 21909-49-9 500mg $200 2021-12-16 Buy
Activate Scientific AS145988 Ethyl2-(2-methyl-1H-indol-3-yl)acetate 97% 21909-49-9 1g $423 2021-12-16 Buy
American Custom Chemicals Corporation CHM0078178 ETHYL 2-METHYL-3-INDOLEACETATE 95.00% 21909-49-9 1G $691.27 2021-12-16 Buy
American Custom Chemicals Corporation CHM0078178 ETHYL 2-METHYL-3-INDOLEACETATE 95.00% 21909-49-9 5G $1080.57 2021-12-16 Buy
Product number Packaging Price Buy
511161 5g $166 Buy
E940635 500mg $200 Buy
AS145988 1g $423 Buy
CHM0078178 1G $691.27 Buy
CHM0078178 5G $1080.57 Buy

ETHYL 2-METHYL-3-INDOLEACETATE Chemical Properties,Uses,Production

Uses

• ;Reactant for preparation of hydroxamate derivatives as HDAC inhibitor with anticancer activity1• ;Reactant for stereoselective preparation of AG-041R, as a Potent Gastrin/CCK-B Receptor Antagonist2

Uses

  • Reactant for preparation of hydroxamate derivatives as HDAC inhibitor with anticancer activity
  • Reactant for stereoselective preparation of AG-041R, as a Potent Gastrin/CCK-B Receptor Antagonist

General Description

Ethyl 2-methyl-3-indoleacetate, also known as ethyl 2-(2-methyl-1H-indol-3-yl)acetate, is a substituted 1H-indole.

923291-61-6
21909-49-9
Synthesis of ETHYL 2-METHYL-3-INDOLEACETATE from 2-Propenoic acid, 3-[2-[(Z)-(1-(phenylseleno)ethylidene)amino]phenyl]-, ethyl ester

ETHYL 2-METHYL-3-INDOLEACETATE Preparation Products And Raw materials

Raw materials

Preparation Products

ETHYL 2-METHYL-3-INDOLEACETATE Suppliers

Global( 21)Suppliers
Supplier Tel Email Country ProdList Advantage
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 sales@capotchem.com China 18217 66
Shanghai Hanhong Scientific Co.,Ltd. 021-021-64543801 13764082696 2355241799@qq.com China 42982 64
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
Shanghai Anmike Chemical Co. Ltd. 18019252918 sale@amkchem.com China 5633 55
Energy Chemical 021-58432009 400-005-6266 marketing1@energy-chemical.com China 44843 58
Shanghai Haohong Pharmaceutical Co., Ltd. 400-8210725 4008210725 malulu@leyan.com China 39997 58
Bide Pharmatech Ltd. 400-1647117 15221909166 product02@bidepharm.com China 63720 58
Bide Pharmatech Ltd. 400-6005915 sales@picasso-e.com China 39661 58

ETHYL 2-METHYL-3-INDOLEACETATE Spectrum

ETHYL 2-METHYL-3-INDOLEACETATE Ethyl 2-methylindoleacetate Nsc289352 1H-Indole-3-acetic acid, 2-Methyl-, ethyl ester Ethyl 2-methyl-3-indoleacetate 98% ethyl 2-(2-methyl-1H-indol-3-yl)acetate 2-(2-methyl-2-indolyl)acetic acid ethyl ester Ethyl 2-Methyl-1H-indole-3-acetate 21909-49-9 Indoles Heterocyclic Building Blocks Building Blocks Building Blocks C13 to C27 Chemical Synthesis Heterocyclic Building Blocks Indole Building Blocks Heterocyclic Building Blocks Indoles