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β-Piperonyl-acrylsaeure, also known as β-piperonyl acrylate, is a chemical compound with the molecular formula C16H15NO3. It is a colorless to pale yellow liquid that is soluble in organic solvents. β-Piperonyl-acrylsaeure is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its ability to enhance the effectiveness of certain pesticides and is also used in the production of some fragrances and flavorings. The compound is derived from the reaction of piperonyl alcohol with acrylic acid, and its structure features a piperonyl group attached to an acrylate moiety, which contributes to its reactivity and utility in chemical synthesis.

28026-94-0

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28026-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28026-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28026-94:
(7*2)+(6*8)+(5*0)+(4*2)+(3*6)+(2*9)+(1*4)=110
110 % 10 = 0
So 28026-94-0 is a valid CAS Registry Number.

28026-94-0Downstream Products

28026-94-0Relevant academic research and scientific papers

Cobalt-Catalyzed Allylic C(sp3)-H Carboxylation with CO2

Michigami, Kenichi,Mita, Tsuyoshi,Sato, Yoshihiro

supporting information, p. 6094 - 6097 (2017/05/08)

Catalytic carboxylation of the allylic C(sp3)-H bond of terminal alkenes with CO2 was developed with the aid of a Co/Xantphos complex. A wide range of allylarenes and 1,4-dienes were successfully transformed into the linear styrylacetic acid and hexa-3,5-dienoic acid derivatives in moderate to high yields, with excellent regioselectivity. The carboxylation showed remarkable functional group tolerability, so that selective addition to CO2 occurred in the presence of other carbonyl groups such as amide, ester, and ketone. Since styrylacetic acid derivatives can be readily converted into optically active γ-butyrolactones through Sharpless asymmetric dihydroxylation, this allylic C(sp3)-H carboxylation showcases a facile synthesis of γ-butyrolactones from simple allylarenes via short steps.

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