60609-65-6

Usage

Uses

Used in Pharmaceutical Industry:
3',5'-Dimethyl-4'-Methoxyacetophenone is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Chemical Synthesis Processes:
3',5'-Dimethyl-4'-Methoxyacetophenone is used as a reagent in various chemical synthesis processes. Its versatility and reactivity contribute to the production of a wide range of chemical products, including other organic compounds and specialty chemicals.

InChI:InChI=1/C11H14O2/c1-7-5-10(9(3)12)6-8(2)11(7)13-4/h5-6H,1-4H3

Upstream product

• 5325-04-2 1-(4-hydroxy-3,5-dimethylphenyl)ethanone 
• 77-78-1 dimethyl sulfate 
• 1004-66-6 2-methoxy-1,3-dimethylbenzene 
• 75-36-5 acetyl chloride 
• 576-26-1 2.6-dimethylphenol 
• 74-88-4 methyl iodide 
• 876-98-2 2,6-dimethylphenyl acetate 
• 92100-74-8 5-(tert-butyl)-2-methoxy-1,3-dimethylbenzene 

Downstream Products

• 21553-46-8 4-methoxy-3,5-dimethylbenzoic acid 
• 1023741-06-1 5-(4-methoxy-3,5-dimethylphenyl)-3H-1,2-dithiole-3-thione 
• 110457-67-5 5-ethyl-2-methoxy-1,3-dimethylbenzene 
• 1023740-37-5 5-(3,5-dimethyl-4-methoxy-phenyl)-3H-1,2-dithiol-3-one 
• 1023740-52-4 3-(4-methoxy-3,5-dimethylphenyl)-β-oxo-propanoic acid methyl ester 
• 54119-42-5 3,5-Dimethyl-4-methoxystyren 
• 104216-50-4 (4-methoxy-3,5-dimethylphenyl)acetic acid 
• 92958-71-9 2-Methoxy-5-(1-methyl-1-hydroxy-ethyl)-benzoldicarbonsaeure-(1,3) 
• 107642-70-6 N-(2,6-Dimethyl-phenyl)-N'-[1-(4-methoxy-3,5-dimethyl-phenyl)-eth-(E)-ylidene]-hydrazine 
• 102005-30-1 4-[(4-methoxy-3,5-dimethyl-phenyl)-thioacetyl]-morpholine 

Relevant academic research and scientific papers

Synthesis and preliminary pharmacological evaluation of aryl dithiolethiones with cyclooxygenase-2-selective inhibitory activity and hydrogen sulfide-releasing properties

A series of 5-aryl-1,2-dithiolethiones and 5-aryl-1,2-dithiole-3-ones were investigated as hydrogen sulfide-releasing anti-inflammatory drugs. Generally, phenolic acetophenones were best protected by methoxymethyl groups and the dithiolethione group insta

1,3-Diphenylprop-2-En-1-One Derivative Compounds, Preparation Method Thereof and Uses of Same

The invention relates to substituted 1,3-diphenylprop-2-en-1-one derivative compounds, pharmaceutical and/or cosmetic compositions containing same, and the applications thereof in therapeutics and cosmetics. The invention also relates to a method for prep

DITHIOLE COMPOUNDS AS COX INHIBITORS

A compound of formula (I) wherein: R1 and R2 are the same or different and are independently selected from H and a shielding group; X and Y are each independently selected from N and CH; R3 is hydroxy, alkoxy, acyloxy or a

Friedel-Crafts ipso-Acylations of 2-Substituted 4-tert-Butylanisoles and p-tert-Butylmethoxymetacyclophanes

Acylation of 1,n-bis(5-tert-butyl-2-methoxyphenyl)alkanes 6 with acid chloride or acid anhydride in the presence of Lewis acids afforded only the product arizing from two-fold ipso-acylation at the tert-butyl groups; similar reaction of 1,2-bis(5-tert-butyl-2-methoxy-3-methylphenyl)alkanes 8 led only to the recovery of the starting compounds, thus differing from the nitration of 8 with fuming HNO3 at room temperature which affords in quantitative yield the selective ipso-nitration product at the tert-butyl groups.However, the ipso-acylation reactions of 5,13-di-tert-butyl-8,16-dimethoxymeta-cyclophane 15 led to the first-reported direct introduction of an acyl group due to a through-space electronic interaction with the opposing benzene ring.In contrast the selective ipso-acylation reaction was not observed in the case of the larger ring sized macrocyclic meta-cyclophane, p-tert-butyltetramethoxycalix(4)arene.

SIGMATROPIC REARRANGEMENT OF ARYLHYDRAZONES FOLLOWED BY 1,2-SHIFT OF AN ARYL GROUP. VII

Arylhydrazones of ethyl 4-methoxy-3,5-dimethylphenylglyoxylate and 4-methoxy-3,5-dimethylacetophenone rearrange in hot polyphosphoric acid to give biphenyl derivatives arising from a sigmatropic rearrangement followed by an aryl group 1,2-shift.Stru