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1-(7-chloro-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol is a complex organic compound with a molecular formula of C28H34ClNO2. It is characterized by a quinoline ring system, which is a fused ring structure consisting of a benzene ring and a pyridine ring. The compound features a 7-chloro substituent on the quinoline, a 2-phenyl group, and a 4-yl group that connects to a 2-(dihexylamino)ethanol moiety. The dihexylamino group consists of two hexyl chains attached to a nitrogen atom, which is connected to the ethanol group. This chemical structure suggests potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules, given its unique combination of functional groups and potential for interaction with biological targets.

5431-82-3

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5431-82-3 Usage

Quinoline derivative

A type of chemical compound based on the quinoline ring structure
Quinoline derivatives are a class of compounds derived from the quinoline ring, which is a tricyclic, nitrogen-containing structure.

Chloro substituent

A chlorine atom attached to the quinoline ring
The presence of a chloro substituent introduces a chlorine atom to the quinoline ring, which can affect the compound's reactivity and properties.

Phenyl substituent

A phenyl group (C6H5) attached to the quinoline ring
The phenyl substituent is an aromatic ring that can influence the compound's stability, solubility, and interaction with other molecules.

Dihexylamino group

A dialkylamine group with two hexyl chains (C6H13) attached to the nitrogen atom
The dihexylamino group is a bulky, hydrophobic group that can affect the compound's solubility and interaction with biological targets.

Ethanol group

A hydroxyl (OH) group attached to an ethyl chain (C2H5)
The ethanol group introduces a polar, hydrophilic moiety to the molecule, which can influence its solubility and interaction with biological systems.

Potential pharmacological properties

The compound may have biological activities relevant to drug development
This suggests that 1-(7-chloro-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol could be a candidate for further research in medicinal chemistry.

Medicinal chemistry research

The compound is being investigated for its possible applications in the development of new drugs
This indicates that the compound is of interest to researchers due to its potential therapeutic properties.

Biological activities

The specific effects of the compound on biological systems are still under investigation
This means that the compound's interactions with biological targets, such as enzymes, receptors, or cellular pathways, are not yet fully understood.

Potential applications

The compound may be used in the development of new therapeutic agents or as a research tool
This highlights the compound's potential value in the field of drug discovery and development, as well as its use in understanding biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5431-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5431-82:
(6*5)+(5*4)+(4*3)+(3*1)+(2*8)+(1*2)=83
83 % 10 = 3
So 5431-82-3 is a valid CAS Registry Number.

5431-82-3SDS

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 1-(7-chloro-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol,hydrochloride

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:5431-82-3 SDS

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