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392-41-6

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392-41-6 Usage

General Description

Methyl trifluoroacrylate, also known as 2,3,3-trifluoropropenoic acid methyl ester, is a chemical compound with the formula C4H3F3O2. It is characterized by a highly reactive acrylic double bond, which makes it a valuable starting material for various polymerization reactions. The product of these reactions, poly(methyl trifluoroacrylate), is a fluoropolymer that displays unique properties, including outstanding chemical resistance and high-temperature stability. Methyl trifluoroacrylate is a colorless, highly volatile liquid at room temperature and must be handled with care due to its acutely toxic and corrosive nature.

Check Digit Verification of cas no

The CAS Registry Mumber 392-41-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 392-41:
(5*3)+(4*9)+(3*2)+(2*4)+(1*1)=66
66 % 10 = 6
So 392-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F3O2/c1-9-4(8)2(5)3(6)7/h1H3

392-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl trifluoroacrylate

1.2 Other means of identification

Product number -
Other names methyl 2,3,3-trifluoroprop-2-enoate

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:392-41-6 SDS

392-41-6Relevant articles and documents

Direct Transformation of Tetrafluoroethylene to Trifluorovinylzinc via sp2C-F Bond Activation

Kikushima, Kotaro,Etou, Yuusuke,Kamura, Ryohei,Takeda, Ippei,Ito, Hideki,Ohashi, Masato,Ogoshi, Sensuke

supporting information, p. 8167 - 8172 (2020/11/02)

Trifluorovinylzinc is a common synthetic intermediate for trifluorovinyl derivatives, including α,β,β-trifluorostyrenes and hexafluorobutadiene. Here, we report a novel synthetic approach for the formation of trifluorovinylzinc chloride via a C-F bond activation of tetrafluoroethylene (TFE), which is an industrially cost-effective bulk feedstock with a negligible GWP. The present system provides a practical synthetic route to various trifluorovinyl derivatives with very low energy consumption.

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