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Methyl 2-(3-bromoquinolin-6-yl)acetate is a versatile chemical compound belonging to the class of acetate esters. It features a methyl group, a bromine atom, and a quinoline ring structure, which contributes to its reactivity and potential applications in various fields. Its IUPAC name is methyl 2-(3-bromo-6-quinolinyl)acetate. The presence of the quinoline ring, a common structural motif in many bioactive compounds, may also endow it with potential biological activities and pharmacological properties.

1022091-89-9

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1022091-89-9 Usage

Uses

Used in Pharmaceutical Synthesis:
Methyl 2-(3-bromoquinolin-6-yl)acetate is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to introduce the quinoline moiety into different chemical structures makes it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, Methyl 2-(3-bromoquinolin-6-yl)acetate serves as a crucial component in the synthesis of various agrochemicals. Its reactivity and the presence of the quinoline ring allow for the creation of compounds with pesticidal, herbicidal, or other agricultural applications.
Used in Fine Chemicals Production:
Methyl 2-(3-bromoquinolin-6-yl)acetate is utilized as a building block in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. Its versatile reactivity and the presence of the quinoline ring enable the synthesis of a wide range of fine chemicals with specific properties and applications.
Used in Organic Compounds Synthesis:
Due to its reactivity and the presence of the quinoline ring, Methyl 2-(3-bromoquinolin-6-yl)acetate is employed in the synthesis of various organic compounds. It can be used to create a diverse array of molecules with different functional groups and properties, suitable for various applications in research, industry, and other fields.
Potential Biological Activities and Pharmacological Properties:
The presence of the quinoline ring in Methyl 2-(3-bromoquinolin-6-yl)acetate may also confer potential biological activities and pharmacological properties. Further research and development could explore its potential as a therapeutic agent or as a lead compound for the discovery of new drugs with various applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 1022091-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,2,0,9 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1022091-89:
(9*1)+(8*0)+(7*2)+(6*2)+(5*0)+(4*9)+(3*1)+(2*8)+(1*9)=99
99 % 10 = 9
So 1022091-89-9 is a valid CAS Registry Number.

1022091-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(3-bromoquinolin-6-yl)acetate

1.2 Other means of identification

Product number -
Other names Methyl 2-(3-bromoquinolin-6-yl)acetate

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:1022091-89-9 SDS

1022091-89-9Relevant academic research and scientific papers

HETEROCYCLIC KINASE MODULATORS

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Page/Page column 115-116, (2009/01/20)

The present disclosure provides heterocyclic protein kinase modulators and methods of using these compounds to treat diseases mediated by kinase activity.

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