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Diethyl 2,6-dihydroxy-4-phenyl-2,6-bis(trifluoromethyl)tetrahydro-2H-pyran-3,5-dicarboxylate is a complex organic compound with the molecular formula C20H20F6O8. It is a derivative of tetrahydro-2H-pyran, featuring a phenyl group at the 4-position and two trifluoromethyl groups at the 2 and 6 positions. The compound also has two hydroxyl groups at the 2 and 6 positions, and two ester groups at the 3 and 5 positions, which are connected to diethyl groups. This molecule is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of more complex molecules. Its unique structure, with the combination of hydroxyl, trifluoromethyl, and ester groups, contributes to its reactivity and versatility in chemical transformations.

3449-44-3

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3449-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3449-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,4 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3449-44:
(6*3)+(5*4)+(4*4)+(3*9)+(2*4)+(1*4)=93
93 % 10 = 3
So 3449-44-3 is a valid CAS Registry Number.

3449-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2,6-dihydroxy-4-phenyl-2,6-bis(trifluoromethyl)oxane-3,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3449-44-3 SDS

3449-44-3Downstream Products

3449-44-3Relevant academic research and scientific papers

Reactions of alkyl 2-benzylidene-2-polyfluoroacylacetates with N,N-dinucleophiles

Pryadeina,Burgart,Kodess,Saloutin,Chupakhin

, p. 1261 - 1266 (2004)

Alkyl 2-benzylidene-2-polyfluoroacylacetates react with urea and thiourea to yield 5-ethoxycarbonyl-4-fluoroalkyl-4-hydroxy-6-phenylhexahydropyrimidin-2- ones and -2-thiones and with guanidine sulfate to form 2-amino-5-ethoxycarbonyl- 4-fluoroalkyl-6-phenyl-1,6-dihydropyrimidines and 3,6-diethoxycarbonyl-2,7- difluoroalkyl-4,5-diphenyl-4,5-dihydro-1H-pyrido[1,2-a]pyrimidines, and they react with phenylhydrazine to afford 4-alkoxycarbonyl-3-fluoroalkyl-3-hydroxy-1, 5-diphenylpyrazolidines. Hydrazine hydrate catalyzes the formation of 3,5-diethoxycarbonyl-2,6-difluoroalkyl-2,6-dihydroxy-4-phenyltetrahydropyrans. When treated with anhydrous hydrazine and o-phenylenediamine, these esters cleave to form the products of condensation of fluoroacyl ester and benzaldehyde with diamines.

Synthesis of 2,6-bis(fluoroalkyl)-2,6-dihydroxytetrahydro-2H-pyran-3,5- dicarboxylates from aldehydes and fluorinated β-oxo esters in the presence of ionic liquid-K2CO3 as catalytic system

Zlotin,Kryshtal',Zhdankina,Ignatenko,Burgart,Saloutin,Chupakhin

experimental part, p. 468 - 473 (2010/07/06)

An efficient procedure has been developed for the synthesis of 4-substituted 2,6-bis(fluoroalkyl)-2,6-dihydroxytetrahydro-2H-pyran-3,5- dicarboxylates by reactions of aldehydes with fluorine-containing β-oxo esters in heterogeneous catalytic system 1-buty

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