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139399-66-9

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139399-66-9 Usage

General Description

3-Chloroquinolin-8-amine is a chemical compound with the molecular formula C9H7ClN2. It is a derivative of quinoline, a heterocyclic aromatic compound, and contains a chlorine atom attached to the 3-position and an amino group attached to the 8-position of the quinoline ring. 3-CHLOROQUINOLIN-8-AMINE has potential applications in the pharmaceutical industry, particularly in the synthesis of novel drugs and medicinal compounds. Its unique structure and functional groups make it a valuable building block for the development of new pharmaceutical agents with potential therapeutic effects. Its properties and reactivity make it a target for further research and development in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 139399-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,9 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139399-66:
(8*1)+(7*3)+(6*9)+(5*3)+(4*9)+(3*9)+(2*6)+(1*6)=179
179 % 10 = 9
So 139399-66-9 is a valid CAS Registry Number.

139399-66-9SDS

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 3-chloroquinolin-8-amine

1.2 Other means of identification

Product number -
Other names 3-chloro-[8]quinolylamine

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:139399-66-9 SDS

139399-66-9Downstream Products

139399-66-9Relevant articles and documents

Effect of 3-subsitution of quinolinehydroxamic acids on selectivity of histone deacetylase isoforms

Mehndiratta, Samir,Chen, Mei-Chuan,Chao, Yuh-Hsuan,Lee, Cheng-Hsin,Liou, Jing-Ping,Lai, Mei-Jung,Lee, Hsueh-Yun

, p. 74 - 84 (2020/11/10)

A series of 3-subsituted quinolinehydroxamic acids has been synthesised and evaluated for their effect on human lung cancer cell line (A549), human colorectal cancer cell line (HCT116) and HDAC isoforms 1, 2, 6, and 8. The results indicated that substitut

Improved Syntheses of Some Monohloro- and Monobromo-8-quinolinols

Gershon, Herman,Clarke, Donald D.

, p. 935 - 942 (2007/10/02)

Procedures were developed for the preparation of the 2-, 3-, 4-, and 6-monosubstituted chloro and bromo 8-quinolinols which afforded greater yields and/or reduced the number of steps in the preparation. 100 MHz 1H-NMR spetra for the 12 possible monochloro

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