60609-65-6

Basic information

• Product Name: 3',5'-DIMETHYL-4'-METHOXYACETOPHENONE
• Synonyms: 3',5'-DIMETHYL-4'-METHOXYACETOPHENONE;1-(4-methoxy-3,5-dimethylphenyl)ethanone;4-Acetyl-2,6-dimethylanisole
• CAS NO: 60609-65-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Mol File: 60609-65-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 47-48 °C(Solv: ethyl ether (60-29-7))
• Boiling Point: 109°C/0.1mm
• Flash Point: 126.5°C
• Appearance: /
• Density: 1.004g/cm³
• Vapor Pressure: 0.00195mmHg at 25°C
• Refractive Index: 1.504
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3',5'-DIMETHYL-4'-METHOXYACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3',5'-DIMETHYL-4'-METHOXYACETOPHENONE(60609-65-6)
• EPA Substance Registry System: 3',5'-DIMETHYL-4'-METHOXYACETOPHENONE(60609-65-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 60609-65-6(Hazardous Substances Data)

Usage

General Description

3',5'-Dimethyl-4'-Methoxyacetophenone is a chemical compound that belongs to the class of organic compounds known as acetophenones, which are aromatic compounds containing a ketone substituted by a phenyl group and an acyl group. The presence of the methoxy group and the dimethyl groups influence the compound’s properties, including its reactivity and solubility. It is structurally featured by a carbonyl group (C=O) bonded to one carbon atom of a phenyl ring. It is known for its high melting and boiling points due to intermolecular forces. As with many chemicals, it must be handled with care due to potential hazards associated with it. The compound may be used in the pharmaceutical industry and has potential applications in other chemical synthesis processes.

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 
• 92100-74-8 5-(tert-butyl)-2-methoxy-1,3-dimethylbenzene 
• 576-26-1 2.6-dimethylphenol 
• 876-98-2 2,6-dimethylphenyl acetate 
• 74-88-4 methyl iodide 

Downstream Products

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

Relevant articles and documents

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

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

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