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106877-17-2

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106877-17-2 Usage

General Description

2-Methyl-4-(trifluoromethyl)pyridine, also known as MTP, is a chemical compound with the formula C7H6F3N. It is a clear, colorless liquid that is used as a building block in the synthesis of various pharmaceuticals and agrochemicals. MTP is commonly employed as an intermediate in the production of herbicides, insecticides, and fungicides, due to its strong and selective activity against a range of pests and weeds. Its trifluoromethyl group gives it unique chemical properties, making it a valuable resource in the development of new compounds with potential applications in the field of crop protection and pharmaceuticals. However, it is important to use MTP safely and responsibly, as it can be hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 106877-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106877-17:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*7)+(2*1)+(1*7)=142
142 % 10 = 2
So 106877-17-2 is a valid CAS Registry Number.

106877-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-4-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-methyl-4-trifluoromethylpyridine

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:106877-17-2 SDS

106877-17-2Downstream Products

106877-17-2Relevant articles and documents

The Stronger the Better: Donor Substituents Push Catalytic Activity of Molecular Chromium Olefin Polymerization Catalysts

Enders, Markus,Hansen, Helge-Boj,Wadepohl, Hubert

, p. 11084 - 11093 (2021)

The donor strength of bifunctional pyridine-cyclopentadienyl ligands was altered systematically by the introduction of donating groups in the para-position of the pyridine. In the resulting chromium complexes an almost linear correlation between donor str

Copper-mediated perfluoroalkylation of heteroaryl bromides with (phen)CuRF

Mormino, Michael G.,Fier, Patrick S.,Hartwig, John F.

, p. 1744 - 1747 (2014/04/17)

The attachment of perfluoroalkyl groups onto organic compounds has been a major synthetic goal over the past several decades. Previously, our group reported phenanthroline-ligated perfluoroalkyl copper reagents, (phen)CuR F, which react with aryl iodides and aryl boronates to form the corresponding benzotrifluorides. Herein the perfluoroalkylation of a series of heteroaryl bromides with (phen)CuCF3 and (phen)CuCF 2CF3 is reported. The mild reaction conditions allow the process to tolerate many common functional groups. Perfluoroethylation with (phen)CuCF2CF3 occurs in somewhat higher yields than trifluoromethylation with (phen)CuCF3, creating a method to generate fluoroalkyl heteroarenes that are less accessible from trifluoroacetic acid derivatives.

Reactions of Trifluoromethyl Bromide and Related Halides: Part 10. Perfluoroalkylation of Aromatic Compounds induced by Sulphur Dioxide Radical Anion Precursors

Tordeux, Marc,Langlois, Bernard,Wakselman, Claude

, p. 2293 - 2299 (2007/10/02)

Perfluoroalkylation of electron-rich aromatic compounds with trifluoromethyl bromide, or long-chain perfluoroalkyl iodides, was performed in the presence of sodium dithionite or zinc-sulphur dioxide.This alkylation occurred at the ortho and para positions relative to the amino or hydroxy substitutent.Pyrroles were perfluoroalkylated regioselectively at the 2-position.This alkylation was interpreted as a radical aromatic substitution; the formation of the perfluoroalkyl radical can be induced by a single-electron transfer from sulphur dioxide radical anion to the perfluoroalkyl halide.

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