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3-Cyclohexylidenpropionsaeure-methylester, also known as methyl 3-cyclohexylidenepropionate, is an organic compound with the chemical formula C10H16O2. It is a colorless liquid with a fruity, apple-like odor and is used as a flavoring agent in the food and beverage industry. The compound is synthesized by the reaction of cyclohexanone and methyl acrylate, resulting in a cyclohexylidene ring structure. It is known for its stability and ability to impart a pleasant aroma to various products, making it a valuable ingredient in the creation of artificial fruit flavors.

3426-57-1

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3426-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3426-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3426-57:
(6*3)+(5*4)+(4*2)+(3*6)+(2*5)+(1*7)=81
81 % 10 = 1
So 3426-57-1 is a valid CAS Registry Number.

3426-57-1Downstream Products

3426-57-1Relevant academic research and scientific papers

Copper-catalyzed vinylogous aerobic oxidation of unsaturated compounds with air

Zhang, Hai-Jun,Schuppe, Alexander W.,Pan, Shi-Tao,Chen, Jin-Xiang,Wang, Bo-Ran,Newhouse, Timothy R.,Yin, Liang

, p. 5300 - 5310 (2018/04/24)

A mild and operationally simple copper-catalyzed vinylogous aerobic oxidation of β,γ- and α,β-unsaturated esters is described. This method features good yields, broad substrate scope, excellent chemo- and regioselectivity, and good functional group tolerance. This method is additionally capable of oxidizing β,γ- and α,β-unsaturated aldehydes, ketones, amides, nitriles, and sulfones. Furthermore, the present catalytic system is suitable for bisvinylogous and trisvinylogous oxidation. Tetramethylguanidine (TMG) was found to be crucial in its role as a base, but we also speculate that it serves as a ligand to copper(II) triflate to produce the active copper(II) catalyst. Mechanistic experiments conducted suggest a plausible reaction pathway via an allylcopper(II) species. Finally, the breadth of scope and power of this methodology are demonstrated through its application to complex natural product substrates.

Chiral Selenide-Catalyzed Enantioselective Allylic Reaction and Intermolecular Difunctionalization of Alkenes: Efficient Construction of C-SCF3 Stereogenic Molecules

Liu, Xiang,Liang, Yaoyu,Ji, Jieying,Luo, Jie,Zhao, Xiaodan

supporting information, p. 4782 - 4786 (2018/04/17)

New approaches for the synthesis of enantiopure trifluoromethylthiolated molecules by chiral selenide-catalyzed allylic trifluoromethylthiolation and intermolecular difunctionalization of unactivated alkenes are disclosed. In these transformations, functi

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