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1,1,2,2-tetrafluoro-3-(vinyloxy)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29819-80-5

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29819-80-5 Usage

Physical state

Colorless and odorless liquid

Uses

a. Solvent
b. Precursor in the synthesis of various fluorinated compounds

Chemical structure

Contains four fluorine atoms and a vinyloxy group

Reactivity

Highly reactive due to the presence of fluorine atoms and vinyloxy group

Applications

a. Industrial applications
b. Refrigerant
c. Component in the manufacturing of polymers and plastics

Environmental impact

Low toxicity and low environmental impact

Safety

Preferred choice in many industrial applications due to its low toxicity and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 29819-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,1 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29819-80:
(7*2)+(6*9)+(5*8)+(4*1)+(3*9)+(2*8)+(1*0)=155
155 % 10 = 5
So 29819-80-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H6F4O/c1-2-10-3-5(8,9)4(6)7/h2,4H,1,3H2

29819-80-5SDS

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 3-ethenoxy-1,1,2,2-tetrafluoropropane

1.2 Other means of identification

Product number -
Other names EINECS 249-879-4

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:29819-80-5 SDS

29819-80-5Relevant academic research and scientific papers

Free Radical Hydrophosphorylation of Fluoroalkyl Vinyl Ethers: Synthesis of Fluoroalkyl Phosphonates

Apartsyn, K. A.,Gusarova, N. K.,Khil’ko, M. Ya.,Kireeva, V. V.,Kolyvanov, N. A.,Nedolya, N. A.,Oparina, L. A.,Saprygina, V. N.,Trofimov, B. A.

, p. 614 - 618 (2020)

Abstract: An effective method for the synthesis of dialkyl [2-(polyfluoroalkoxy)ethyl]phosphonates by free radical hydrophosphorylation of fluoroalkyl vinyl ethers with dialkyl (H)-phosphonates was developed. The reaction proceeds in the presence of catalytic amounts of azabisisobutyric acid dinitrile (AIBN) (150°C, 2 h, portionwise addition of AIBN) to afford the target fluoroalkyl phosphonates in up to 85% isolated yield.

SYNTHESIS AND SOME PROPERTIES OF THE VINYL ETHERS OF POLYFLUORINATED ALCOHOLS

Trofimov, B. A.,Khil'ko, M. Ya.,Nedolya, N. A.,Demanov, Yu. K.,Vyalykh, E. P.

, p. 647 - 651 (2007/10/02)

The vinylation of polyfluoroalkanols by acetylene under pressure was investigated with various catalysts (cadmium acetate, potassium alkoxides and hydroxide).In the presence of basic catalysts, irrespective of the reaction conditions, the yield of the fluorovinyl ethers is not greater than 5-12percent.In the presence of cadmium acetate the yield of the ethers is 50-64percent.The effect of various factors (solvents, amount of catalyst, complexing additives, reaction time) on the degree of reaction is discussed.The vinyl ethers of polyfluorinated alcohols do not exhibit anomaliesin the reactions with carbixylic acids, alcohols, and thiols.

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