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4-(4-Chlorostyryl)quinoline is an organic compound characterized by a quinoline ring, which is a tricyclic aromatic system, and a 4-chlorostyryl group attached to it. The quinoline ring is a heterocyclic compound with a benzene ring fused to a pyridine ring, and the 4-chlorostyryl group is a vinylbenzene derivative with a chlorine atom at the 4-position. 4-(4-Chlorostyryl)quinoline is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to handle this chemical with care, as it may have specific safety and health considerations due to the presence of a chlorine atom, which can affect its stability and potential toxicity.

4594-89-2

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4594-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4594-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4594-89:
(6*4)+(5*5)+(4*9)+(3*4)+(2*8)+(1*9)=122
122 % 10 = 2
So 4594-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H12ClN/c18-15-9-6-13(7-10-15)5-8-14-11-12-19-17-4-2-1-3-16(14)17/h1-12H

4594-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-chlorophenyl)ethenyl]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 -
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More Details:4594-89-2 SDS

4594-89-2Downstream Products

4594-89-2Relevant academic research and scientific papers

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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