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2-(4-phenylbutyl)quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5426-20-0

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5426-20-0 Usage

Quinoline derivative

Yes

Class of organic compounds

Quinolines and derivatives

Uses

Synthesis of pharmaceuticals, research reagent in biochemical laboratories, potential anti-cancer and anti-inflammatory properties, potential applications in organic electronics

Unique properties

Electronic and optical properties

Further research needed

Yes

Check Digit Verification of cas no

The CAS Registry Mumber 5426-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5426-20:
(6*5)+(5*4)+(4*2)+(3*6)+(2*2)+(1*0)=80
80 % 10 = 0
So 5426-20-0 is a valid CAS Registry Number.

5426-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-phenylbutyl)quinoline

1.2 Other means of identification

Product number -
Other names -

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:5426-20-0 SDS

5426-20-0Downstream Products

5426-20-0Relevant academic research and scientific papers

Nickel-Catalyzed Dehydrogenation of N-Heterocycles Using Molecular Oxygen

Banerjee, Debasis,Bera, Atanu,Bera, Sourajit

supporting information, (2020/09/02)

Herein, an efficient and selective nickel-catalyzed dehydrogenation of five- and six-membered N-heterocycles is presented. The transformation occurs in the presence of alkyl, alkoxy, chloro, free hydroxyl and primary amine, internal and terminal olefin, trifluoromethyl, and ester functional groups. Synthesis of an important ligand and the antimalarial drug quinine is demonstrated. Mechanistic studies revealed that the cyclic imine serves as the key intermediate for this stepwise transformation.

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