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8-Bromo-7-methoxyquinoline is a chemical compound with the molecular formula C10H8BrNO. It is a derivative of quinoline, featuring a quinoline ring with a bromine atom at the 8th position and a methoxy group at the 7th position. 8-Bromo-7-methoxyquinoline is recognized for its potential biological activities, such as antimicrobial, antitumor, and antioxidant properties, and is also considered for its applications in the development of fluorescent dyes and organic electronic materials.

36023-06-0

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36023-06-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
8-Bromo-7-methoxyquinoline is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, leveraging its unique chemical structure to create new compounds with therapeutic or pesticidal properties.
Used in Antimicrobial Applications:
8-Bromo-7-methoxyquinoline is utilized as an antimicrobial agent, exhibiting activity against a range of microorganisms, which makes it a valuable component in the development of new antimicrobial drugs to combat resistant strains.
Used in Antitumor Applications:
As an antitumor agent, 8-Bromo-7-methoxyquinoline is employed for its potential to inhibit tumor growth, making it a candidate for further research and development in oncology.
Used in Antioxidant Applications:
8-Bromo-7-methoxyquinoline is used as an antioxidant, which can help in protecting cells from oxidative damage, a factor in the development of various diseases and aging.
Used in Fluorescent Dyes Development:
8-Bromo-7-methoxyquinoline is used as a component in the development of fluorescent dyes, capitalizing on its chemical properties to create dyes with specific fluorescent characteristics for use in research and diagnostic applications.
Used in Organic Electronic Materials:
8-Bromo-7-methoxyquinoline is utilized in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its potential electronic properties that can enhance device performance.

Check Digit Verification of cas no

The CAS Registry Mumber 36023-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36023-06:
(7*3)+(6*6)+(5*0)+(4*2)+(3*3)+(2*0)+(1*6)=80
80 % 10 = 0
So 36023-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO/c10-8-7(12)4-3-6-2-1-5-11-9(6)8/h1-5,12H

36023-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Bromo-7-Methoxyquinoline

1.2 Other means of identification

Product number -
Other names 8-bromo-7-methoxyquinoline

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:36023-06-0 SDS

36023-06-0Downstream Products

36023-06-0Relevant articles and documents

NOVEL COMPOUND, PHOTOACID GENERATOR CONTAINING THE COMPOUND, AND PHOTOSENSITIVE RESIN COMPOSITION CONTAINING THE PHOTOACID GENERATOR

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, (2018/12/05)

PROBLEM TO BE SOLVED: To provide a nonionic photoacid generator with high acid generation quantum yield. SOLUTION: The present invention provides a compound represented by formula (2) (where, ring Ar is a benzene ring, naphthalene ring, thiophene ring or

A self-contained photoacid generator for super acid based on photochromic terarylene

Li, Ruiji,Nakashima, Takuya,Kawai, Tsuyoshi

, p. 4339 - 4341 (2017/04/21)

A self-contained photoacid generator for super acid along with the photoinduced 6π-electrocyclization reaction of the terarylene backbone is demonstrated. The photoinitiated cationic polymerization of epoxy-monomers is achieved with an efficient photochem

Kinetic Resolution of Axially Chiral 5- or 8-Substituted Quinolines via Asymmetric Transfer Hydrogenation

Wang, Jie,Chen, Mu-Wang,Ji, Yue,Hu, Shu-Bo,Zhou, Yong-Gui

supporting information, p. 10413 - 10416 (2016/09/04)

An efficient kinetic resolution of axially chiral 5- or 8-substituted quinoline derivatives was developed through asymmetric transfer hydrogenation of heteroaromatic moiety, simultaneously obtaining two kinds of axially chiral skeletons with up to 209 of selectivity factor. This represents the first successful application of asymmetric transfer hydrogenation of heteroaromatics in kinetic resolution of axially chiral biaryls.

MODULATORS OF CXCR7

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Page/Page column 53, (2010/06/11)

Compounds having formula (I) or pharmaceutically acceptable salts, hydrates or N-oxides thereof are provided and are useful for binding to CXCR7, and treating diseases that are dependent, at least in part, on CXCR7 activity. Accordingly, the present inven

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