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139399-66-9

3-Chloroquinolin-8-amine, a derivative of quinoline with the molecular formula C9H7ClN2, is a heterocyclic aromatic compound featuring a chlorine atom at the 3-position and an amino group at the 8-position of the quinoline ring. Its unique structure and functional groups contribute to its potential as a valuable building block in the pharmaceutical industry for the synthesis of novel drugs and medicinal compounds, with properties and reactivity that make it a target for further research and development in medicinal chemistry and drug discovery.

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  • 139399-66-9 Structure

  • Basic information

    1. Product Name: 3-CHLOROQUINOLIN-8-AMINE
    2. Synonyms: 3-CHLOROQUINOLIN-8-AMINE
    3. CAS NO:139399-66-9
    4. Molecular Formula: C9H7ClN2
    5. Molecular Weight: 178.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 139399-66-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-CHLOROQUINOLIN-8-AMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-CHLOROQUINOLIN-8-AMINE(139399-66-9)
    11. EPA Substance Registry System: 3-CHLOROQUINOLIN-8-AMINE(139399-66-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 139399-66-9(Hazardous Substances Data)

139399-66-9 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloroquinolin-8-amine is used as a chemical intermediate for the synthesis of novel drugs and medicinal compounds, leveraging its unique structure and functional groups to develop new pharmaceutical agents with potential therapeutic effects.
Used in Medicinal Chemistry Research:
3-Chloroquinolin-8-amine serves as a subject of study in medicinal chemistry, where its properties and reactivity are explored to enhance understanding of its potential applications and to innovate in drug discovery processes.

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

Regiodivergent Visible Light-Induced C–H Functionalization of Quinolines at C-5 and C-8 under Metal-, Photosensitizer- and Oxidant-Free Conditions

Arockiam, Percia Beatrice,Guillemard, Lucas,Wencel-Delord, Joanna

, p. 2571 - 2579 (2017/08/16)

A general strategy towards the selective perfluoroalkylation of quinoline derivatives at C-5 and C-8 is described. This exceptionally mild radical transformation, compatible with a large panel of substrates, does not require any transition metal catalysts or oxidants. Outstandingly, visible light photoinduction using simple household bulbs, in the absence of a photosensitizer, is the unique activation mode. Further importance of this reaction relies on its capacity to functionalize selectively both C-5 and C-8 positions of quinolines. This transformation, perfectly fulfilling green chemistry requirements, allows a truly practical and straightforward access to a variety of unprecedented functionalized amino- and amidoquinoline skeletons, presenting attractive features for medicinal and agrochemical industry. (Figure presented.).

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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