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5443-82-3

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5443-82-3 Usage

Chemical structure

Contains a quinoline core with a 4-methoxyphenyl group attached at the 2-position and an amine group at the 3-position.

Family

Quinoline family

Potential applications

Medicinal chemistry and drug development

Pharmacological properties

Exhibits properties of interest to researchers

Use in organic synthesis

Can be used as a building block to create other functionalized quinoline derivatives

Scientific value

Specific biological and chemical properties make it a valuable target for further study and exploration in various scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 5443-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5443-82:
(6*5)+(5*4)+(4*4)+(3*3)+(2*8)+(1*2)=93
93 % 10 = 3
So 5443-82-3 is a valid CAS Registry Number.

5443-82-3SDS

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 2-(4-methoxyphenyl)quinolin-3-amine

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5443-82-3 SDS

5443-82-3Relevant articles and documents

Modular Synthesis of Polysubstituted Quinolin-3-amines by Oxidative Cyclization of 2-(2-Isocyanophenyl)acetonitriles with Organoboron Reagents

Wang, Shihui,Xu, Jian,Song, Qiuling

supporting information, p. 6789 - 6794 (2021/09/02)

Polysubstituted quinolin-3-amines are vital structural motifs because of their broad biological activities as well as versatile transformational abilities. However, they are not easily accessible. We disclose a protocol with Mn(III) acetate as a mild one-

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