38459-58-4

Basic information

• Product Name: Methanone, cyclohexyl(4-hydroxyphenyl)-
• CAS NO: 38459-58-4
• Molecular Formula: C13H16O2
• Molecular Weight: 204.269
• Mol File: 38459-58-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Methanone, cyclohexyl(4-hydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, cyclohexyl(4-hydroxyphenyl)-(38459-58-4)
• EPA Substance Registry System: Methanone, cyclohexyl(4-hydroxyphenyl)-(38459-58-4)

Safety Data

• Hazardous Substances Data: 38459-58-4(Hazardous Substances Data)

Upstream product

• 7469-80-9 cyclohexyl 4-methoxyphenyl ketone 
• 110-82-7 cyclohexane 
• 120743-99-9 p-[(tert-butyldimethylsilyl)oxy]benzaldehyde 
• 931-48-6 2-cyclohexylacetylene 
• 108-95-2 phenol 
• 3954-12-9 phenyl cyclohexanecarboxylate 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 98-89-5 Cyclohexanecarboxylic acid 
• 100-66-3 methoxybenzene 

Downstream Products

• 147540-48-5 4-(Quinolin-2-yl-methoxy)phenyl cyclohexyl ketone 
• 1393654-93-7 C₁₃H₁₄Br₂O₂ 
• 1539286-81-1 C₁₄H₁₅F₃O₄S 
• 1160829-08-2 C₃₅H₄₃NO₆S 

Relevant articles and documents

One-pot formal dehydrogenative ketone synthesis from aldehydes and non-activated hydrocarbons

Ketones are a fundamental functionality found throughout a range of natural and synthetic compounds, making their synthesis essential throughout the chemical disciplines. Herein, we describe a one-pot synthesis of ketones via decatungstate-mediated formal dehydrogenative coupling between aldehydes and non-activated hydrocarbons. A variety of substituted benzaldehydes and cycloalkanes could be used in the optimized reaction to produce the desired ketones in moderate yields. The decatungstate photocatalyst functions in two reactions in this synthesis, catalyzing both the coupling and oxidation steps of the process. Notably, the reaction displays both high atom economy and sustainability, as it uses light and oxygen as key energy sources.

An improved synthesis of hydroxy aryl ketones by fries rearrangement with methanesulfonic acid/methanesulfonic anhydride

Methanesulfonic acid treated with methanesulfonic anhydride effectively mediates the Fries rearrangement of aryl esters to give hydroxy aryl ketones with high yields. Georg Thieme Verlag Stuttgart · New York.

Synthesis and biochemical evaluation of a series of trifluoromethanesulfonate derivatives of 4 hydroxyphenyl ketones - Probes of the active site of type 1 and 3 of the 17β-hydroxysteroid dehydrogenase family of enzymes

In an effort to aid the design of 'dual-inhibitors' of types 1 and 3 of the 17β-hydroxysteroid dehydrogenase (17β-HSD), we report the synthesis, biochemical evaluation and rationalisation of the inhibitory activity of trifluoromethanesulfonate derivatives of 4-hydroxyphenyl ketone-based compounds which were found to be weak inhibitors of types 1 and 3.