37722-51-3

Upstream product

• 84654-70-6 trans-2-(4-methoxybenzyl)cyclohexyl acetate 
• 37722-64-8 2-(4-methoxybenzyl)cyclohexan-1-one 
• 108-94-1 cyclohexanone 
• 1125-99-1 1-(1-Cyclohexen-1-yl)pyrrolidine 
• 84654-70-6 cis-2-(4-methoxybenzyl)cyclohexyl acetate 

Downstream Products

• 84654-70-6 cis-2-(4-methoxybenzyl)cyclohexyl acetate 
• 860617-83-0 (1R,2R)-2-(4-methoxybenzyl)cyclohexyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 860617-87-4 (1S,2S)-2-(4-methoxybenzyl) cyclohexyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 84654-70-6 trans-2-(4-methoxybenzyl)cyclohexyl acetate 
• 860617-89-6 (1R,2S)-2-(4-methoxybenzyl)cyclohexyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 860617-85-2 (1S,2R)-2-(4-methoxybenzyl)cyclohexyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 112066-40-7 (1R,2S)-2-(4-methoxybenzyl)cyclohexyl acetate 
• 125136-36-9 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,2R)-2-(4-methoxy-benzyl)-cyclohexyl ester 
• 125224-45-5 trans-(1S,2R)-(+)-2-(4-methoxybenzyl)-1-cyclohexanol 
• 112066-34-9 (1R,2S)-2-(4-methoxybenzyl)cyclohexan-1-ol 
• 950835-56-0 (1S,2R)-2-(4-methoxybenzyl)cyclohexyl butanoate 
• 874292-31-6 (1S,2R)-2-(4-methoxybenzyl)cyclohexyl acetate 
• 84654-71-7 Isobutyric acid (1S,2R)-2-(4-methoxy-benzyl)-cyclohexyl ester 
• 84654-72-8 2,2-Dimethyl-propionic acid (1S,2R)-2-(4-methoxy-benzyl)-cyclohexyl ester 

Relevant academic research and scientific papers

Application of ionic liquids in enzymic resolution by hydrolysis of cycloalkyl acetates

A comparative study was performed in the enzymic resolution of the isomers of 2-(4-methoxybenzyl)cyclohexyl acetates 1 and 2. The investigation consisted in application of three commercially available lipases (Novozyme 435, Lipozyme IM and non-immobilized

Synthesis and structure-activity relationships of juvenoids derived from 2-(4-hydroxybenzyl)cycloalkan-1-ones

Juvenoids 16-30, 32, 36, 38-41, 44-46, and 49-56 containing carbamate, carbonate, and urea moieties in the molecule were synthesized and subjected to a biological screening. Carbamate juvenoids 1-4 were used as reference compounds for a detailed structure-activity study of their analogues. A clear relationship between the nature of the side chain functional group and the biological activity was found. Surprisingly, not only the juvenoids 1,4 but also 38-41, the compounds with a reversed carbamate N,O-substitution pattern, showed very promising biological activity. In contrast, the carbonate and urea derivatives displayed a remarkably low activity. The relationship between the size and substitution at atoms C(2) and C(3) of the saturated ring and the biological activity is very complex and is still not completely understood.

CONFORMATION STUDIES OF ISOMERIC 1-ACYLOXY-2-(4-METHOXYBENZYL)-CYCLOHEXANES BY 1H NMR SPECTTOSCOPY

The conformation of the cyclohexane ring and the p-methoxybenzyl substituent in the series of isomeric 1-acyloxy-2-(4-methoxybenzyl)cyclohexanes was studied by means of 1H NMR spectroscopy.In all the substances investigated the cyclohexane ring assumes ch