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1-(7-chloro-6-methoxy-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol is a complex organic compound with a molecular formula of C28H36ClNO3. 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 and 6-methoxy substitution pattern on the quinoline nucleus, which may influence its electronic properties and potential biological activity. The 2-phenyl group attached to the quinoline ring provides additional structural complexity and may contribute to its pharmacological profile. The molecule also includes a 2-(dihexylamino)ethanol moiety, which consists of two hexylamine groups attached to an ethanol backbone. This part of the molecule likely contributes to its solubility and potential interactions with biological targets. Overall, this chemical is a member of a class of compounds that may have applications in medicinal chemistry, particularly in the development of new drugs targeting various diseases and conditions.

5463-40-1

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5463-40-1 Usage

Chemical family

Belongs to the family of quinoline derivatives.

Structural features

Composed of a quinoline ring with a chlorine substituent and a methoxy group, a phenyl group attached to the quinoline ring, an ethanol moiety, and a dihexylamino group.

Molecular weight

Approximately 487.05 g/mol (calculated from the molecular formula)

Appearance

Likely a solid or oily liquid, depending on the conditions (not specified in the material)

Solubility

Soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO) (not specified in the material, but common for similar compounds)

Pharmacological applications

Has potential pharmacological applications due to its structural features (not specified in the material, but inferred from the mention of biological activities)

Biological activities

May exhibit various biological activities (not specified in the material, but inferred from the mention of potential pharmacological applications)

Further research

Additional research and studies are necessary to fully understand the properties and potential uses of this chemical (not specified in the material, but a common statement for compounds with potential applications)

Synthesis

The synthesis of 1-(7-chloro-6-methoxy-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol likely involves multiple steps, including the formation of the quinoline ring, introduction of the chlorine and methoxy substituents, attachment of the phenyl group, and the addition of the ethanol and dihexylamino moieties (not specified in the material, but a common process for complex organic compounds)

Check Digit Verification of cas no

The CAS Registry Mumber 5463-40-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5463-40:
(6*5)+(5*4)+(4*6)+(3*3)+(2*4)+(1*0)=91
91 % 10 = 1
So 5463-40-1 is a valid CAS Registry Number.

5463-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(7-chloro-6-methoxy-2-phenylquinolin-4-yl)-2-(dihexylamino)ethanol,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(7-CHLORO-6-METHOXY-2-PHENYLQUINOLIN-4-YL)-2-(DIHEXYLAMINO)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:5463-40-1 SDS

5463-40-1Upstream product

5463-40-1Downstream Products

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