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METHYL 2-METHYL-6-(TRIFLUOROMETHYL)NICOTINATE, a chemical compound with the molecular formula C11H9F3N2O2, is a derivative of nicotinic acid. It features a methyl group and a trifluoromethyl group, which contribute to its unique chemical properties. METHYL 2-METHYL-6-(TRIFLUOROMETHYL)NICOTINATE is known for its potential therapeutic and pesticidal properties, making it a valuable asset in pharmaceutical and agrochemical industries.

205582-88-3

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205582-88-3 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 2-METHYL-6-(TRIFLUOROMETHYL)NICOTINATE is used as a therapeutic agent for its potential antiviral and anti-inflammatory properties. Its unique chemical structure allows it to target specific biological pathways, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Agrochemical Industry:
METHYL 2-METHYL-6-(TRIFLUOROMETHYL)NICOTINATE is used as a pesticidal agent for its insecticidal and fungicidal activities. Its ability to control pests and diseases in crops can contribute to increased agricultural productivity and crop protection.
The trifluoromethyl group in METHYL 2-METHYL-6-(TRIFLUOROMETHYL)NICOTINATE may enhance its bioactivity and metabolic stability, making it a valuable compound in drug discovery and agricultural applications. This feature allows for the development of more effective and longer-lasting treatments and pesticides, ultimately benefiting both human health and agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 205582-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,5,8 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 205582-88:
(8*2)+(7*0)+(6*5)+(5*5)+(4*8)+(3*2)+(2*8)+(1*8)=133
133 % 10 = 3
So 205582-88-3 is a valid CAS Registry Number.

205582-88-3SDS

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 methyl 2-methyl-6-(trifluoromethyl)pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2-methyl-6-trifluoromethyl-nicotinic acid methyl ester

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:205582-88-3 SDS

205582-88-3Relevant articles and documents

Method for preparation of 6-trifluoromethylpyridine-3-carboxylic acid derivatives from 4,4,4-trifluoro-3-aminobutanoates

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Paragraph 0047-0048, (2015/01/18)

The invention discloses a method for the preparation of substituted 6-trifluoromethylpyridine-3-carboxylic acid derivatives starting from 4,4,4-trifluoro-3-aminobutanoates and proceeding via enamines and dihydropyridinones.

METHOD FOR PREPARATION OF 6-TRIFLUOROMETHYLPYRIDINE-3-CARBOXYLIC ACID DERIVATIVES FROM TRIFLUOROACETYLACETIC ACID

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Page/Page column 11, (2015/02/02)

The invention discloses a method for the preparation of 6- trifluoromethylpyridine-3-carboxylic acid derivatives (I) from trifluoroacetylacetic acid (II) and orthoesters (III), and their use for the preparation of pharmaceutical, chemical or agro-chemical products.

Method for preparation of 6-trifluoromethylpyridine-3-carboxylic acid derivatives

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Paragraph 0043, (2014/12/09)

The invention discloses a method for the preparation of substituted 6-trifluoromethylpyridine-3-carboxylic acid derivatives starting from 1,1,1-trifluoroacetone or from synthetic equivalents of 1,1,1-trifluoroacetone.

Radical-based regioselective C-H functionalization of electron-deficient heteroarenes: Scope, tunability, and predictability

O'Hara, Fionn,Blackmond, Donna G.,Baran, Phil S.

supporting information, p. 12122 - 12134 (2013/09/02)

Radical addition processes can be ideally suited for the direct functionalization of heteroaromatic bases, yet these processes are only sparsely used due to the perception of poor or unreliable control of regiochemistry. A systematic investigation of fact

Triazolopyridine cannabinoid receptor 1 antagonists

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Page/Page column 78, (2008/06/13)

The present application describes compounds according to Formula I, pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents, and methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents. The compounds have the following general formula: including all prodrugs, solvates, pharmaceutically acceptable salts and stereoisomers, wherein R1, R2, R3, R4 and R5 are described herein.

Triazolopyrimidine cannabinoid receptor 1 antagonists

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Page/Page column 42, (2010/11/25)

The present application describes compounds according to both Formulas I and II, pharmaceutical compositions comprising at least one compound according to either Formula I or II and optionally one or more additional therapeutic agents, and methods of treatment using the compounds according to Formulas I and II both alone and in combination with one or more additional therapeutic agents. The compounds have the following general formulas: including all prodrugs, solvates, pharmaceutically acceptable salts and stereoisomers, wherein R1, R2, R3, R4 and R5 are described herein.

Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators

Lahm, George P.,Selby, Thomas P.,Freudenberger, John H.,Stevenson, Thomas M.,Myers, Brian J.,Seburyamo, Gilles,Smith, Ben K.,Flexner, Lindsey,Clark, Christopher E.,Cordova, Daniel

, p. 4898 - 4906 (2007/10/03)

A novel class of anthranilic diamides has been discovered with exceptional insecticidal activity on a range of Lepidoptera. These compounds have been found to exhibit their action by release of intracellular Ca2+ stores mediated by the ryanodine receptor. The discovery, synthesis, structure-activity, and biological results are presented.

A simple and convenient synthetic method for α -trifluoromethylpyridines

Okada, Etsuji,Kinomura, Tatsuhiko,Higashiyama, Yukio,Takeuchi, Hiroshi,Hojo, Masaru

, p. 129 - 132 (2007/10/03)

β-Trifluoroacetylvinylamine (1) reacted easily with various active methylene compounds in the presence of trifluoroacetic acid under mild conditions to give α-trifluoromethylpyridines (2) in moderate to high yields.

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