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2859-55-4

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2859-55-4 Usage

General Description

4-[2-(4-methoxyphenyl)ethenyl]quinoline is a chemical compound belonging to the quinoline family. It is characterized by a quinoline core structure with an ethenyl side chain and a 4-methoxyphenyl substituent. 4-[2-(4-methoxyphenyl)ethenyl]quinoline has potential applications in the field of organic and medicinal chemistry, where it may be used as a building block for the synthesis of novel pharmaceuticals, dyes, or other organic compounds. Its unique structure and properties make it a valuable tool for researchers and chemists studying the design and synthesis of new molecules with various biological or chemical activities. Additionally, the presence of an ethenyl group and a methoxyphenyl group may give this compound specific reactivity or pharmacological properties that could be of interest for further investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 2859-55-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2859-55:
(6*2)+(5*8)+(4*5)+(3*9)+(2*5)+(1*5)=114
114 % 10 = 4
So 2859-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H15NO/c1-20-16-10-7-14(8-11-16)6-9-15-12-13-19-18-5-3-2-4-17(15)18/h2-13H,1H3

2859-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-methoxyphenyl)ethenyl]quinoline

1.2 Other means of identification

Product number -
Other names 4-<4-Methoxyphenylazo>-1-naphthylamin

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:2859-55-4 SDS

2859-55-4Relevant articles and documents

Nickel-Catalyzed Dehydrogenation of N-Heterocycles Using Molecular Oxygen

Banerjee, Debasis,Bera, Atanu,Bera, Sourajit

, (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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