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Methyl 3,3-difluoroacrylate is a colorless liquid chemical compound with the molecular formula C4H4F2O2. It is an ester derivative of acrylic acid, featuring a methyl group attached to the 3,3-difluoroacrylate moiety. METHYL 3,3-DIFLUOROACRYLATE is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its reactivity, it is essential to handle methyl 3,3-difluoroacrylate with caution, as it can cause skin and eye irritation, respiratory issues, and potential harm to the environment. It is also important to store and transport this chemical in a controlled manner to prevent accidents and ensure safety.

406-05-3

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406-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406-05-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 406-05:
(5*4)+(4*0)+(3*6)+(2*0)+(1*5)=43
43 % 10 = 3
So 406-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H4F2O2/c1-8-4(7)2-3(5)6/h2H,1H3

406-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,3-difluoroprop-2-enoate

1.2 Other means of identification

Product number -
Other names methyl difluoroacrylate

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:406-05-3 SDS

406-05-3Relevant academic research and scientific papers

Reformatsky Reaction of Methyl 2-Bromo-3,3,3-trifluoropropanoate. A Synthetic Method for α-Trifluoromethyl-β-hydroxy Esters

Yokozawa, Tsutomu,Ishikawa, Nobuo,Nakai, Takeshi

, p. 1971 - 1974 (2007/10/02)

The Reformatsky reagent, prepared from the title bromo-ester and zinc powder in dioxane, is found to be thermally stable enough to undergo addition reactions with aldehydes to afford the α-trifluoromethyl-β-hydroxy esters in high yields.The unique reactiv

(TRIFLUOROMETHYL)KETENE SILYL ACETAL AS AN EQUIVALENT TO THE TRIFLUOROPROPIONIC ESTER ENOLATE: PREPARATION AND ALDOL-TYPE REACTIONS WITH ACETALS

Yokozawa, Tsutomu,Nakai, Takeshi,Ishikawa, Nobuo

, p. 3987 - 3990 (2007/10/02)

The title reagent, readily prepared from methyl β,β,β-trifluoropropionate with trimethylsilyl triflate, is shown to react with a broad variety of acetals to provide the corresponding α-CF3 β-alkoxy esters in good yields.

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