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2-(Trifluoromethyl)acrylic acid, also known as 2-(trifluoromethyl)-2-propenoic acid, is a synthetic chemical compound with the molecular formula C4H3F3O2. It is a colorless liquid with a pungent odor and is soluble in water. 2-(trifluoromethyl)acrylic acid is an important building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique reactivity and properties. It features a trifluoromethyl group, which imparts lipophilicity and metabolic stability to the molecules in which it is incorporated. The acrylic acid moiety allows for further functionalization and polymerization, making it a versatile intermediate in organic synthesis.

4423-82-9

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4423-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4423-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4423-82:
(6*4)+(5*4)+(4*2)+(3*3)+(2*8)+(1*2)=79
79 % 10 = 9
So 4423-82-9 is a valid CAS Registry Number.

4423-82-9Relevant academic research and scientific papers

Palladium-Catalyzed Hydrocarboxylation of Alkynes with Formic Acid

Hou, Jing,Xie, Jian-Hua,Zhou, Qi-Lin

supporting information, p. 6302 - 6305 (2015/05/20)

A palladium-catalyzed hydrocarboxylation of alkynes with formic acid has been developed. The method provides acrylic acid and derivatives in good yields with high regioselectivity without the need to handle toxic CO gas. Nontoxic: Acrylic acids are an important chemical feedstock. The title reaction provides acrylic acid and derivatives in good yields with high regioselectivities without the need to handle toxic CO gas.

Regioselective control of the thiocarbonylation of terminal acetylenes with arylthiols catalyzed by Pd(II) and diphosphine ligands

El Ali,Tijani,El-Ghanam,Fettouhi

, p. 1567 - 1570 (2007/10/03)

Control of the regioselective thiocarbonylation of terminal acetylenes 1a-e with arylthiols 2a,b was successfully achieved by using Pd(OAc)2 and 1,4-bis(diphenylphosphino)butane (dppb), or 1,3-bis(diphenylphosphino)propane (dppp), as catalysts.

Reactions of Ozone with 2,3-Di-tert-butyl-1,3-butadiene in Solution and on Solid Supports

Griesbaum, Karl,Volpp, Willi

, p. 1795 - 1800 (2007/10/02)

Reactions of the title compounds 1 with ozone in pentane, on silica gel, or on alumina gave no ozonides, but the corresponding mono- and diketone 3 and 4, mono- and di-epoxide 5 and 7, as well as epoxy ketone 6.Ozonation of 1 on polyethylene afforded mono-ozonide 9 and further ozonation of the latter gave an epoxy ozonide 10.

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