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2,3-Dimethoxy-5-(trifluoromethyl)pyridine is a pyridine derivative with the molecular formula C9H8F3NO2. It features a pyridine ring with two methoxy groups and a trifluoromethyl group attached, which contributes to its unique reactivity and properties. This chemical compound is recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a building block in organic synthesis, enhancing the characteristics of organic molecules. Furthermore, it has been investigated for its potential biological activities, showing promise as a drug candidate for various medical applications.

124432-61-7

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124432-61-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-Dimethoxy-5-(trifluoromethyl)pyridine is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the development of new compounds with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 2,3-Dimethoxy-5-(trifluoromethyl)pyridine serves as a key intermediate in the production of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness and selectivity, leading to improved agricultural outcomes.
Used in Organic Synthesis:
As a building block in organic synthesis, 2,3-Dimethoxy-5-(trifluoromethyl)pyridine is utilized for the creation of a wide range of organic molecules. Its ability to modify the reactivity and properties of these molecules makes it a valuable component in the synthesis of various organic compounds for different applications.
Used in Drug Discovery:
2,3-Dimethoxy-5-(trifluoromethyl)pyridine has been studied for its potential biological activities, making it a candidate for drug discovery. Its unique structure and properties may offer new avenues for the development of therapeutic agents targeting a variety of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 124432-61-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,3 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124432-61:
(8*1)+(7*2)+(6*4)+(5*4)+(4*3)+(3*2)+(2*6)+(1*1)=97
97 % 10 = 7
So 124432-61-7 is a valid CAS Registry Number.

124432-61-7SDS

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 2,3-Dimethoxy-5-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2,3-dimethoxy-5-(4-fluorophenylthio)-1,4-naphthoquinone

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:124432-61-7 SDS

124432-61-7Downstream Products

124432-61-7Relevant academic research and scientific papers

Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst

Cheung, Chi Wai,Buchwald, Stephen L.

supporting information, p. 3998 - 4001 (2013/09/02)

A general method for the Pd-catalyzed coupling of methanol with (hetero)aryl halides is described. The reactions proceed under mild conditions with a wide range of aryl and heteroaryl halides to give methyl aryl ethers in high yield.

N-cyanomethyl-2-pyridinone insecticides

-

, (2008/06/13)

Substituted N-cyanomethyl-2-pyridinones were prepared by the reaction of alkali metal substituted-2-pyridinates with monohaloacetonitriles and found to possess insecticidal properties. The alkali metal substituted-2-pyridinates can be preformed or prepared from the corresponding 2-halopyridines or 2-pyridinols in the reaction medium. N-cyanomethyl-3-fluoro-5-(trifluoromethyl)-2-pyridinone, for example, was prepared from 2,3-difluoro-5-(trifluoromethyl)pyridine and found to control aster leafhoppers both on contact and systemically.

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