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4-Chloro-6-methoxy-quinoline-3-carbonitrile is a specialized chemical compound belonging to the class of organochlorines. It is known for its distinctive characteristics due to the presence of a quinoline ring, a nitrile group (-CN), a chloro group, and a methoxy group (-OCH3). These functional groups enhance its reactivity and solubility in organic solvents, making it ideal for various chemical reactions. However, it is important to handle and store 4-CHLORO-6-METHOXY-QUINOLINE-3-CARBONITRILE in controlled environments due to its potential harmful effects when in contact with skin or if ingested or inhaled.

13669-62-0

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13669-62-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-6-methoxy-quinoline-3-carbonitrile is used as an intermediate compound for the synthesis of various pharmaceutical drugs. Its unique structure and reactivity make it a valuable building block in the development of new medications.
Used in Chemical Reactions:
4-CHLORO-6-METHOXY-QUINOLINE-3-CARBONITRILE is used as a reactant in various chemical reactions, taking advantage of its nitrile and chloro groups to form new chemical entities. Its versatility in reactions contributes to the synthesis of a wide range of products in the chemical industry.
Used in Research and Development:
4-Chloro-6-methoxy-quinoline-3-carbonitrile is employed as a research compound in academic and industrial laboratories. Its unique properties make it an interesting subject for studying the effects of different functional groups on the reactivity and properties of quinoline-based compounds. This research can lead to the discovery of new applications and uses for 4-CHLORO-6-METHOXY-QUINOLINE-3-CARBONITRILE in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 13669-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,6 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13669-62:
(7*1)+(6*3)+(5*6)+(4*6)+(3*9)+(2*6)+(1*2)=120
120 % 10 = 0
So 13669-62-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H7ClN2O/c1-15-8-2-3-10-9(4-8)11(12)7(5-13)6-14-10/h2-4,6H,1H3

13669-62-0SDS

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 4-chloro-6-methoxyquinoline-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarbonitrile,4-chloro-6-methoxy

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:13669-62-0 SDS

13669-62-0Downstream Products

13669-62-0Relevant academic research and scientific papers

Hetero-aromatic compound and its use in medicine

-

, (2019/07/04)

The invention provides a hetero-aromatic compound or a stereisomer, geometric isomer, tautomer, despinner, nitrogen oxide, hydrate, solvate, metabolite, metabolism precursor and pharmaceutically acceptable salt or prodrug thereof, which is used for treating proliferative diseases. The invention also discloses a pharmaceutical composition containing the compound and an application of the compound or pharmaceutical composition thereof in preparation of a medicine for treating proliferative diseases.

INHIBITORS OF DNA GYRASE FOR THE TREATMENT OF BACTERIAL INFECTIONS

-

, (2014/05/07)

The present invention relates to compounds which specifically inhibit bacterial DNA Gyrase and can be used for the treatment of respiratory tract infections.

ANTIBACTERIAL AGENTS

-

Page/Page column 61, (2010/02/15)

Naphthalene, quinoline, quinoxaline and naphthyridine derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

Synthesis and structure-activity relationships of 3-cyano-4(phenoxyanilino)quinolines as MEK (MAPKK) inhibitors

Zhang, Nan,Wu, Biqi,Powell, Dennis,Wissner, Allan,B. Floyd, Middleton,D. Kovacs, Eleonora,Toral-Barza, Lourdes,Kohler, Constance

, p. 2825 - 2828 (2007/10/03)

A series of 3-cyano-4-(phenoxyanilino)cyanoquinolines has been prepared as MEK (MAP kinase kinase) inhibitors. The best activity is seen with alkoxy groups at both the 6- and 7-positions. The lead compounds show low nanomolar IC50's against MAP kinase kinase, and have potent inhibitory activity in tumor cells. (C) 2000 Elsevier Science Ltd.

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