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Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester is a chemical compound characterized by its molecular formula C7H5F7O2. It is an ethyl ester of propanoic acid, featuring a unique structure with four fluorine atoms and a trifluoromethyl group. Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester is widely recognized for its role as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.

1526-49-4

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1526-49-4 Usage

Uses

Used in Pharmaceutical Industry:
Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester is utilized as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the synthesis of drug molecules, contributing to the advancement of new treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester serves as a key intermediate in the synthesis of various agrochemicals. Its properties allow for the creation of effective and targeted pest control solutions, enhancing crop protection and contributing to sustainable agricultural practices.
Used in Specialty Chemicals Production:
Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester is also employed in the production of specialty chemicals, where its unique structure and reactivity are leveraged to create high-performance materials for diverse applications.
Used as a Solvent in Organic Synthesis:
Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester is used as a solvent in organic synthesis processes, providing a medium for chemical reactions to occur. Its stability and compatibility with a range of reactants make it a preferred choice in various synthesis procedures.
Used as a Reagent in Chemical Reactions:
Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester functions as a reagent in specific chemical reactions, facilitating the formation of desired products and enhancing the efficiency of synthesis processes.
It is crucial to handle Propanoic acid, 2,3,3,3-tetrafluoro-2-(trifluoromethyl)-, ethyl ester with care due to its potential hazards if not used properly, ensuring safety and proper disposal practices in the industries where it is applied.

Check Digit Verification of cas no

The CAS Registry Mumber 1526-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1526-49:
(6*1)+(5*5)+(4*2)+(3*6)+(2*4)+(1*9)=74
74 % 10 = 4
So 1526-49-4 is a valid CAS Registry Number.

1526-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,2,3,3,3-tetrafluoro-2-(trifluoromethyl)-,ethyl 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:1526-49-4 SDS

1526-49-4Relevant academic research and scientific papers

Estimation of hydrocarbon solubilities in hydrofluorocarbons

Puy, Michael Van Der,Poss, Andrew J.,Persichini, Phillip J.,Ellis, Lois A. S.

, p. 215 - 224 (1994)

A new solubility parameter, SP, for hydrofluorocarbons (HFCs) has been developed (SP = 1.175 ln(np) + 0.025H - 0.063F - 0.028α - 0.018β where np depends on the molar volume and the molar refractivity; H and F are the number of hydrogens and fluorines, respectively, in the molecule; and α and β are the respective numbers of H-C-F and H-C-C-F connections).Values of SP have been used to predict if an HFC would be a good solvent for various hydrocarbons at 25 deg C.Within an isomeric HFC family, the individual HFCs having the greatest solvency for hydrocarbons were those having the maximum separation of fluorines from hydrogens.Hildebrand solubility parameters, δ, are compared with the semi-empirical SP values.Syntheses for 10 new compounds are given: 3,3,4,4,5,5,6,6,7,7-decafluorononane, 1,1,1,2-tetrafluoro-2-(trifluoromethyl)-3-methylbutane, 1,1,1,2,2-pentafluoro-3-methylbutane, 1,1,1,2,2,3,3,4,4-nonafluoro-5-methylhexane, 1,1,1,2,2,3,3,4,4-nonafluoroheptane, 1,1,1,2-tetrafluoro-2-(trifluoromethyl)butane, 1,1,1-trifluoro-3-(trifluoromethyl)butane, 1,1,1,2,2,3,3,5-octafluorohexane, 1,1,1,2,2-pentahydroperfluorooctane and 1,1,1,2,2-pentahydroperfluorodecane.

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