54771-60-7

Basic information

• Product Name: 4-ACETYL-2-METHOXYPHENYL ACETATE
• Synonyms: Phenol, 4-acetyl-2-methoxy, acetate;LABOTEST-BB LT00012613;1-(4-ACETOXY-3-METHOXYPHENYL)ETHANONE;4-ACETYLACETOVANILLONE;4-ACETOXY-3-METHOXYACETOPHENONE;4-ACETYL-2-METHOXYPHENYL ACETATE;4-Acethyl-2-methoxyphenyl acetete;Acetic acid 4-acetyl-2-methoxyphenyl ester
• CAS NO: 54771-60-7
• Molecular Formula: C₁₁H₁₂O₄
• Molecular Weight: 208.21058
• Product Categories: Aromatic Acetophenones & Derivatives (substituted)
• Mol File: 54771-60-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: 54-57 °C(lit.)
• Boiling Point: 294.7°C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 0.00159mmHg at 25°C
• Refractive Index: 1.506
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-ACETYL-2-METHOXYPHENYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ACETYL-2-METHOXYPHENYL ACETATE(54771-60-7)
• EPA Substance Registry System: 4-ACETYL-2-METHOXYPHENYL ACETATE(54771-60-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 54771-60-7(Hazardous Substances Data)

Usage

General Description

4-ACETYL-2-METHOXYPHENYL ACETATE is a chemical compound with the molecular formula C11H12O4. It is a derivative of acetic acid and belongs to the class of phenols. 4-ACETYL-2-METHOXYPHENYL ACETATE is commonly used in the synthesis of pharmaceuticals and is known for its analgesic and anti-inflammatory properties. It has been investigated as a potential ingredient in pain relief medications and is also used in the production of fragrances and flavoring agents. Additionally, 4-ACETYL-2-METHOXYPHENYL ACETATE is also utilized in the chemical industry for its role as a precursor in the synthesis of various organic compounds.

InChI:InChI=1/C11H12O4/c1-7(12)9-4-5-10(15-8(2)13)11(6-9)14-3/h4-6H,1-3H3

Upstream product

• 108-24-7 acetic anhydride 
• 24332-96-5 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 64-19-7 acetic acid 

Downstream Products

• 91671-30-6 2-(4-acetoxy-3-methoxyphenyl)-4-methyl-4-penten-2-ol 
• 82491-66-5 Acetic acid 4-[2-(4-acetoxy-3-methoxy-phenyl)-1,2-dihydroxy-1-methyl-propyl]-2-methoxy-phenyl ester 
• 91671-24-8 ethyl 2-(4-acetoxy-3-methoxyphenyl)-2-hydroxybutanoate 
• 172757-22-1 R-1-(4-acetoxy-3-methoxyphenyl)ethanol 
• 160925-73-5 β-chloroacetoguaiacone acetate 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 91012-60-1 1-(4-hydroxy-3-methoxy-phenyl)-2-methylamino-ethanone 
• 881-95-8 dl-metanephrine hydrochloride 
• 383382-42-1 3,4-dihydroxy-2-nitroacetophenone 
• 1260785-45-2 1-(4-hydroxy-3-methoxy-2-nitro-phenyl)-ethanone 

Relevant articles and documents

NOVEL BENZOFURAN TYPE DERIVATIVES, A COMPOSITION COMPRISING THE SAME FOR TREATING OR PREVENTING COGNITIVE DYSFUNCTION AND THE USE THEREOF

The present invention relates to the novel benzofuran derivatives, the preparation thereof and the composition comprising the same. The benzofuran derivatives of the present invention showed potent inhibiting activity of beta-amyloid aggregation and cell cytotoxicity resulting in stimulating the proliferation of neuronal cells as well as recovering activity of memory learning injury caused by neuronal cell injury using transformed animal model with beta-amyloid precursor gene, therefore the compounds can be useful in treating or preventing cognitive function disorder.

NOVEL BENZOFURAN TYPE DERIVATIVES, A COMPOSITION COMPRISING THE SAME FOR TREATING OR PREVENTING COGNITIVE DYSFUNCTION AND THE USE THEREOF

The present invention relates to the novel benzofuran derivatives, the preparation thereof and the composition comprising the same. The benzofuran derivatives of the present invention showedpotent inhibiting activity of beta-amyloid aggregation and cell cytotoxicity resulting in stimulating the proliferation of neuronal cells as well as recovering activity of memory learning injury caused by neuronal cell injury using transformed animal model with beta-amyloid precursor gene, therefore the compounds can be useful in treating or preventing cognitive function disorder.

NOVEL ZWITTERIONIC FLUORESCENT DYES FOR LABELING IN PROTEOMIC AND OTHER BIOLOGICAL ANALYSES

The invention relates to compositions and methods useful in the labeling and identification of proteins. The invention provides for highly soluble zwitterionic dye molecules where the dyes and associated side groups are non-titratable and maintain their net zwitterionic character over a broad pH range, e.g. between pH 3 and 12. These dye molecules find utility in a variety of applications, including use in the field of proteomics.