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1-[7-chloro-2-(4-chlorophenyl)quinolin-4-yl]-2-(dibutylamino)ethanol is a complex organic compound with the molecular formula C27H32Cl2NO. It features a quinoline core, which is a tricyclic aromatic system, with a chlorine atom at the 7-position and a 4-chlorophenyl group attached at the 2-position. The 4-position of the quinoline ring is connected to a side chain that includes a dibutylamino group and an ethanol moiety. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its unique combination of functional groups and aromatic systems. The presence of chlorine atoms and the dibutylamino group may contribute to its reactivity or specific biological activity, although further information on its uses and properties would be required for a comprehensive understanding.

6316-92-3

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6316-92-3 Usage

Chemical compound

A substance formed by a chemical reaction, consisting of a complex molecular structure.

Quinoline ring

A basic structure in the molecule, consisting of a fused six-membered nitrogen-containing ring and a five-membered ring.

Dibutylamino group

A functional group attached to the quinoline ring, consisting of two butyl groups attached to an amine group.

Ethanol moiety

A functional group attached to the molecule, consisting of an ethyl group connected to a hydroxyl group.

Chloroquinoline derivative

A classification of the compound, indicating the presence of chlorine atoms in the quinoline ring.

Two chlorine atoms

The compound contains two chlorine atoms, which may contribute to its biological activity.

Medicinal and pharmacological research

The compound's structural resemblance to known bioactive molecules suggests potential applications in these fields.

Solubility

The dibutylamino group may improve the compound's solubility in various solvents, which is important for drug development.

Pharmacokinetic properties

The dibutylamino group may also influence the compound's absorption, distribution, metabolism, and excretion in the body.

Biological activities

The chloroquinoline scaffold has been associated with various biological activities, such as anti-inflammatory, antimalarial, and anticancer effects.

Further studies needed

More research is required to fully understand the chemical and biological characteristics of 1-[7-chloro-2-(4-chlorophenyl)quinolin-4-yl]-2-(dibutylamino)ethanol.

Check Digit Verification of cas no

The CAS Registry Mumber 6316-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6316-92:
(6*6)+(5*3)+(4*1)+(3*6)+(2*9)+(1*2)=93
93 % 10 = 3
So 6316-92-3 is a valid CAS Registry Number.

6316-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[7-chloro-2-(4-chlorophenyl)quinolin-4-yl]-2-(dibutylamino)ethanol,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-[7-CHLORO-2-(4-CHLOROPHENYL)QUINOLIN-4-YL]-2-(DIBUTYLAMINO)ETHANOL HYDROCHLORIDE

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:6316-92-3 SDS

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