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Home > Encyclopedia > ETHYL 2-METHYL-3-INDOLEACETATE

ETHYL 2-METHYL-3-INDOLEACETATE

ETHYL 2-METHYL-3-INDOLEACETATE structure

ETHYL 2-METHYL-3-INDOLEACETATE 

structure
  • CAS No:

    21909-49-9

  • Formula:

    C13H15NO2

  • Chemical Name:

    ETHYL 2-METHYL-3-INDOLEACETATE

  • Synonyms:

    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

  • Categories:

    Chemical Reagents  >  Organic Reagents

ETHYL 2-METHYL-3-INDOLEACETATE Basic Attributes

217.26

217.11000

289352

DTXSID20314853

2933990090

Characteristics

42.1

2.58190

1.158g/cm3

95 °C(Solv: ethyl ether (60-29-7))

195-196 °C3.5 mm Hg(lit.)

>230 °F

n20/D 1.571(lit.)

1.5E-05mmHg at 25°C

Safety Information

NONH for all modes of transport

3

36/37/38

26-36

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

ETHYL 2-METHYL-3-INDOLEACETATE Use and Manufacturing

• ;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

Computed Properties

Molecular Weight:217.26
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:217.110278721
Monoisotopic Mass:217.110278721
Topological Polar Surface Area:42.1
Heavy Atom Count:16
Complexity:254
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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