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2-IODOTETRAFLUOROETHYL TRIFLUOROMETHYL ETHER is a chemical compound characterized by its highly electronegative tetrafluoroethyl and trifluoromethyl ether groups, which enable it to participate in a variety of chemical reactions. Its highly fluorinated structure makes it a valuable reagent in organic synthesis, particularly for the formation of carbon-fluorine bonds.

1561-52-0

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1561-52-0 Usage

Uses

Used in Pharmaceutical Industry:
2-IODOTETRAFLUOROETHYL TRIFLUOROMETHYL ETHER is used as a reagent for the production of fluorinated compounds, which are beneficial for their improved stability and bioavailability in pharmaceutical applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-IODOTETRAFLUOROETHYL TRIFLUOROMETHYL ETHER serves as a reagent for synthesizing fluorinated compounds that can enhance the effectiveness and environmental stability of agrochemical products.
Used in Materials Science:
2-IODOTETRAFLUOROETHYL TRIFLUOROMETHYL ETHER is utilized as a precursor in the preparation of fluorinated polymers and coatings, which exhibit enhanced chemical and thermal resistance, making them suitable for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1561-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1561-52:
(6*1)+(5*5)+(4*6)+(3*1)+(2*5)+(1*2)=70
70 % 10 = 0
So 1561-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C3F7IO/c4-1(5,11)2(6,7)12-3(8,9)10

1561-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2-tetrafluoro-1-iodo-2-(trifluoromethoxy)ethane

1.2 Other means of identification

Product number -
Other names Trifluormethyl-<1,1,2,2-tetrafluor-2-iod-ethyl>-ether

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:1561-52-0 SDS

1561-52-0Downstream Products

1561-52-0Relevant academic research and scientific papers

Production of tetrafluoroethylene and di-acid

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Paragraph 0099; 0104-0106, (2018/04/03)

[A] having high yield and purity of the di-acid specific structure simple and safe method for manufacturing. General formula [a]: ICF2 CF2 The fuming sulfuric acid is oxidized by ORf [...] shown, general formula: FCOCF2 After obtaining the di-acid ORf shown, the di-acid reaction with hexafluoropropylene oxide, having the general formula FCOCF (CF3 ) OCF2 CF2 As shown in the di-acid ORf production. [Drawing] no

MEASUREMENT OF RATE CONSTANTS AND EQUILIBRIUM CONSTANTS OF RI R + I AND I + RI I2 + R FOR R = C3F7, iso-C3F7, C6F13, CF3OCF2CF2, OR C3F7OCF2CF2

Skorobogatov, G. A.,Dymov, B. P.,Tedeev, R. Sh.

, p. 158 - 165 (2007/10/02)

The method of isothermal pyrolysis of an iodide RI can produce highly accurate data about the equilibrium constants and rate constants of the reactions RI R + I and I + RI R + I2, if the rate constant for recombination R + R -> R2 is known.Data on the absolute rate constants of the thermal dissociation of the iodides C3F7I, iso-C3F7I, C6F13I, CF3O(CF2)2I and C3F7O(CF2)2I, and also for their reaction with atomic iodine were obtained for the first time using this technique.The dissociation energies ED (R-I) are 212+/-2, 201+/-2, 202+/-2, 213+/-2, and 213+/-2 kJ/mole, respectively.

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