2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Base Information

Chemical Name:2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure
CAS No.:76618-89-8
Molecular Formula:C₁₅H₂₀O₃
Molecular Weight:248.322
Hs Code.:

Synonyms:2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Suppliers and Price of 2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemicals and raw materials
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Total 3 raw suppliers

Chemical Property of 2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of 2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

There total 6 articles about 2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

: 76618-88-7
2-cyclohexyl-2-(4-methoxyphenyl)acetonitrile

: 76618-89-8
2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Guidance literature:: With potassium hydroxide;

Reference yield: 43.0%

: 104-01-8
4-Methoxyphenylacetic acid

: 953-91-3
cyclohexyl tosylate

: 76618-89-8
2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

Guidance literature:: 4-Methoxyphenylacetic acid; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

cyclohexyl tosylate; In tetrahydrofuran; hexane; at -78 - 25 ℃; for 13h;
DOI:10.1016/j.bmc.2018.03.023

Reference yield:

: 917-64-6
methyl magnesium iodide

: 76618-89-8
2-Cyclohexyl-2-(p-methoxyphenyl)essigsaeure

: 100-06-1
1-(4-methoxyphenyl)ethanone

Guidance literature:: With diethyl ether; Erhitzen des Reaktionsprodukts mit Kaliumhydrogensulfat und Behandeln des danach isolierten Reaktionsprodukts mit Chrom(VI)-oxid und wss. Essigsaeure;