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1H-Indole, 3,3-diethyl-2,3-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130546-01-9

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130546-01-9 Usage

Structure

An indole derivative with two ethyl groups attached to the 3 position

Physical state

Colorless liquid

Uses

Commonly used in organic synthesis and as a building block for the production of various pharmaceuticals and agrochemicals

Applications

Precursor for the synthesis of dyes, pigments, and perfumes in the chemical industry

Medicinal properties

Potential anti-cancer and anti-inflammatory effects, making it a compound of interest for pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 130546-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,4 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130546-01:
(8*1)+(7*3)+(6*0)+(5*5)+(4*4)+(3*6)+(2*0)+(1*1)=89
89 % 10 = 9
So 130546-01-9 is a valid CAS Registry Number.

130546-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-diethyl-1,2-dihydroindole

1.2 Other means of identification

Product number -
Other names 3,3-diethyl-2,3-dihydro-1H-indole

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:130546-01-9 SDS

130546-01-9Upstream product

130546-01-9Relevant academic research and scientific papers

Et3SiH + KO: T Bu provide multiple reactive intermediates that compete in the reactions and rearrangements of benzylnitriles and indolenines

Arokianathar, Jude N.,Clark, Kenneth F.,Dimitrova, Daniela,Leach, Stuart G.,Murphy, John A.,Poole, Darren L.,Smith, Andrew J.

, p. 12364 - 12370 (2020)

The combination of potassium tert-butoxide and triethylsilane is unusual because it generates multiple different types of reactive intermediates simultaneously that provide access to (i) silyl radical reactions, (ii) hydrogen atom transfer reactions to cl

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