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Ethanone, 1-(3,4-dihydro-2-methoxy-2H-pyran-5-yl)-2,2,2-trifluoro(9CI) is a complex organic chemical compound characterized by an ethanone molecule with a trifluoromethyl group and a 3,4-dihydro-2-methoxy-2H-pyran-5-yl ring. This 9CI compound exhibits a distinctive structure that may confer unique properties, making it a candidate for exploration in various industries, particularly pharmaceutical and agrochemical.
Used in Pharmaceutical Industry:
Ethanone, 1-(3,4-dihydro-2-methoxy-2H-pyran-5-yl)-2,2,2-trifluoro(9CI) is used as a potential active pharmaceutical ingredient for its unique molecular structure that could interact with biological targets in novel ways, leading to the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, Ethanone, 1-(3,4-dihydro-2-methoxy-2H-pyran-5-yl)-2,2,2-trifluoro(9CI) may serve as a key intermediate in the synthesis of new pesticides or herbicides, leveraging its structural features to target specific pests or weeds more effectively and with fewer environmental impacts.
Further research is necessary to fully elucidate the potential uses and effects of Ethanone, 1-(3,4-dihydro-2-methoxy-2H-pyran-5-yl)-2,2,2-trifluoro- (9CI), ensuring its safety and efficacy in practical applications.

220370-51-4

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220370-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220370-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,7 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 220370-51:
(8*2)+(7*2)+(6*0)+(5*3)+(4*7)+(3*0)+(2*5)+(1*1)=84
84 % 10 = 4
So 220370-51-4 is a valid CAS Registry Number.

220370-51-4SDS

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 2,2,2-Trifluoro-1-(2-methoxy-3,4-dihydro-2H-pyran-5-yl)ethanone

1.2 Other means of identification

Product number -
Other names 5-trifluoroacetyl-2-methoxy-3,4-dihydro-2H-pyran

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:220370-51-4 SDS

220370-51-4Relevant academic research and scientific papers

A simple synthetic method for fluorine-containing 4H-pyrano[3,2- d]isoxazoles and 4-cyanoethyl-isoxazoles from 5-trifluoroacetyl-2-methoxy- 3,4-dihydro-2H-pyran with hydroxylamine hydrochloride

Okada, Etsuji,Okumura, Hiroshi,Nishida, Yukihiro,Kitahora, Takeshi

, p. 377 - 384 (1999)

5-Trifluoroacetyl-2-methoxy-3,4-dihydro-2H-pyran (1), prepared from 2- methoxy-3,4-dihydro-2H-pyran with trifluoroacetic anhydride, reacted cleanly with hydroxylamine hydrochloride in alcohol to give fluorine-containing 4H- pyrano[3,2-d]isoxazoles (2a-g) or 4-cyanoethyldihydroisoxazoles (3) selectively in moderate to high yields. Further conversion of 3 into 4- cyanoethylisoxazoles (4) was also described.

Synthesis of 1-Arylethyl-2-arylethylamino-5-trifluoroacetyl-1,2,3,4-tetrahydropyridines and Related Compounds with Potential Cell Efflux Pump Inhibition

Zanatta, Nilo,Lobo, Marcio M.,Dos Santos, Josiane M.,Souza, Laura De A.,De Andrade, Valquiria P.,Bonacorso, Helio G.,Martins, Marcos A. P.

, p. 1776 - 1781 (2015)

This study reports a simple, fast, and efficient method for the synthesis of a new series of 1-arylethyl-2-arylethylamino-5-trifluoroacetyl-1,2,3,4-tetrahydropyridines and related compounds from the reaction of 2-alkoxy-5-trifluoroacetyl-3,4-dihydro-2H-py

Highly chemoselective synthesis of 6-Alkoxy-l-aIkyl(aryl)-3- trifluoroaeetyl-1,4,5,6 tetrahydropyridlines and 1-Alkyl(aryl)-6-anino-3- trifluoroacetyl-1,4,5,6-tetrahydropyridines

Zanatta, Nilo,Fernandes, Liana Da S.,Naehtigall, Fabiane M.,Coelho, Helena S.,Aniaral, Simone S.,Flores, Alex F. C.,Bonacorso, Helio G.,Martins, Marcos A. P.

experimental part, p. 1435 - 1444 (2009/08/07)

A simple and highly chemoselective method for the synthesis of a large series of novel 6-alkoxy-1-alkyl (aryl)-3-trifluoro-acetyl-1,4,5,6- tetrahydropyridines and l-alkyl(aryl)-6-amino-3-trifluoroacetyl-l,4,5,6- tetrahydropyridines, from the reaction of 6

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