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1H-Indole,4-ethoxy-2,3-dihydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220657-56-7

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220657-56-7 Usage

Derivative of indole

A heterocyclic aromatic organic compound

Classification

Secondary amino compound

Structure

Dihydroindole with an ethoxy group attached to the 4th carbon of the indole ring

Usage

Organic synthesis and pharmaceutical research for the development of potential drug candidates

Importance

Valuable compound for the scientific community for its properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 220657-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,5 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 220657-56:
(8*2)+(7*2)+(6*0)+(5*6)+(4*5)+(3*7)+(2*5)+(1*6)=117
117 % 10 = 7
So 220657-56-7 is a valid CAS Registry Number.

220657-56-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxy-2,3-dihydro-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,4-ethoxy-2,3-dihydro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:220657-56-7 SDS

220657-56-7Relevant academic research and scientific papers

Photo-induced rearrangement of 1-ethoxy-2-phenylindole

Yamada, Koji,Somei, Masanori

, p. 2481 - 2484 (2007/10/03)

Photoirradiation of 1-ethoxy-2-phenylindole in methanol afforded 3- and 6-ethoxy-2-phenylindoles. The structural determination of the latter is carried out by direct comparison of its spectral data with those of the authentic 4-, 5-, 6-, and 7-ethoxy-2-phenylindoles, whose syntheses are also included.

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