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Z-2-fluoro-3-(4-methylphenyl)acrylic acid is a chemical compound with the molecular formula C10H9FO2. It is a derivative of acrylic acid, featuring a fluorine atom at the 2-position and a 4-methylphenyl group at the 3-position. Z-2-fluoro-3-(4-methylphenyl)acrylic acid is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used in the preparation of various biologically active molecules, such as anti-inflammatory agents and herbicides. The compound is typically synthesized through various chemical reactions, including condensation and substitution reactions, and is characterized by its distinct chemical properties, such as its reactivity towards nucleophiles and electrophiles.

26928-10-9

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26928-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26928-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,2 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26928-10:
(7*2)+(6*6)+(5*9)+(4*2)+(3*8)+(2*1)+(1*0)=129
129 % 10 = 9
So 26928-10-9 is a valid CAS Registry Number.

26928-10-9Relevant academic research and scientific papers

A novel reaction of β,β'-dihydroxy acids or esters with vanadium(V) trichloride oxide. New entry to the stereoselective synthesis of α-fluoro- α,β-unsaturated acids and esters

Ishihara, Takashi,Shintani, Atsuhiro,Yamanaka, Hiroki

, p. 4865 - 4868 (1998)

β,β'-Dihydroxy carboxylic acids and esters, readily prepared from dibromofluoroacetate and aldehydes, underwent deoxygenation, followed by elimination of aldehyde by the action of vanadium(V) trichloride oxide at the reflux temperature of chlorobenzene fo

Fluorine-containing carboxylic acid compound and preparation method thereof

-

Paragraph 0038-0048; 0058-0061, (2020/09/09)

The invention provides a fluorine-containing carboxylic acid compound and a preparation method and application thereof. The preparation method comprises the steps that a fluorine-containing olefin compound and CO2 react in a solvent in the presence of a c

Copper-Catalyzed Carboxylation of C-F Bonds with CO2

Yan, Si-Shun,Wu, Dong-Shan,Ye, Jian-Heng,Gong, Li,Zeng, Xin,Ran, Chuan-Kun,Gui, Yong-Yuan,Li, Jing,Yu, Da-Gang

, p. 6987 - 6992 (2019/08/26)

An effective Cu-catalyzed selective formal carboxylation of C-F bonds with an atmospheric pressure of CO2 is reported. A variety of gem-difluoroalkenes, gem-difluorodienes, and α-trifluoro-methyl alkenes show high reactivity and selectivity for

An efficient synthesis of (Z)-α-fluorochalcones via the palladium-catalyzed cross-coupling reaction of (Z)-α-fluorocinnamoyl chloride with boronic acids

Eddarir, Said,Kajjout, Mohammed,Rolando, Christian

, p. 1735 - 1738 (2013/03/14)

An efficient synthesis of α-fluorochalcones (1,3-diphenyl-2- fluoroprop-2-en-1-one) based on the Suzuki-Miyaura palladium-catalyzed cross-coupling reaction of arylboronic acids with α-fluorocinnamoyl chlorides in the presence of Cs2CO3/su

Synthetic utilization of 2-chloro-1,1,1,2-tetrafluoroethane

Notsu, Keiji,Zushi, Yasuyuki,Ota, Shin,Kawasaki-Takasuka, Tomoko,Yamazaki, Takashi

, p. 9200 - 9208 (2011/09/19)

β-Substituted α-fluoro-α,β-unsaturated carboxylic acids have been successfully synthesized, usually in a (Z)-stereospecific manner by way of a stepwise or a one-pot three-step procedure starting from 2-chloro-1,1,1,2-tetrafluoroethane (HCFC-124), one of the major byproducts of the industrial process for tetrafluoroethene formation from chlorofluoromethane (HCFC-22). Get some Z's! β-Substituted α-fluoro-α,β- unsaturated carboxylic acids have been successfully synthesized from 2-chloro-1,1,1,2-tetrafluoroethane, one of the major byproducts of tetrafluoroethene formation from chlorofluoromethane. The products are usually obtained with Z stereoselectivity, by either a stepwise or a one-pot three-step procedure (see scheme).

Insight into the reactions of trifluorovinylsilanes with aromatic aldehydes

Kirij, Nataliia V.,Dontsova, Dariya A.,Pavlenko, Natalya V.,Yagupolskii, Yurii L.,Scherer, Harald,Tyrra, Wieland,Naumann, Dieter

experimental part, p. 2267 - 2272 (2009/04/05)

The conditions for the selective addition of trialkyl(trifluorovinyl) silanes to the C=O bond of aromatic aldehydes in the presence of cesium fluoride to give the corresponding "silylated" alcohols in high yields was performed. The reactivity of the "sily

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