97728-73-9

Basic information

• Product Name: 1-(4-broMophenyl)-2-Methoxyethan-1-one
• Synonyms: 1-(4-broMophenyl)-2-Methoxyethan-1-one;1-(4-bromophenyl)-2-methoxyethanone
• CAS NO: 97728-73-9
• Molecular Formula: C₉H₉BrO₂
• Molecular Weight: 229.07056
• Mol File: 97728-73-9.mol
• Article Data: 11

Chemical Properties

• Melting Point: 74-75.5 °C
• Boiling Point: 303.8±27.0 °C(Predicted)
• Appearance: /
• Density: 1.431±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(4-broMophenyl)-2-Methoxyethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-broMophenyl)-2-Methoxyethan-1-one(97728-73-9)
• EPA Substance Registry System: 1-(4-broMophenyl)-2-Methoxyethan-1-one(97728-73-9)

Safety Data

• Hazardous Substances Data: 97728-73-9(Hazardous Substances Data)

Usage

Description

1-(4-bromophenyl)-2-methoxyethan-1-one, a chemical compound with the molecular formula C9H9BrO2, is a derivative of acetophenone featuring a bromine atom and a methoxy group attached to the phenyl ring. This versatile and valuable chemical is widely utilized in the field of organic chemistry due to its unique structural properties.

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-(4-bromophenyl)-2-methoxyethan-1-one is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its presence of bromine and methoxy groups allows for the creation of a diverse range of compounds with potential therapeutic and pesticidal properties.
Used in Perfume and Flavoring Agent Production:
1-(4-bromophenyl)-2-methoxyethan-1-one is also employed as a reagent in the production of perfumes and flavoring agents. The unique combination of bromine and methoxy groups in its structure contributes to the development of novel and distinct scents and flavors for the fragrance and food industries.

Upstream product

• 1738-36-9 2-methoxyacetonitrile 
• 18620-02-5 (4-bromophenyl)magnesium bromide 
• 67-56-1 methanol 
• 99-90-1 para-bromoacetophenone 
• 99-73-0 para-bromophenacyl bromide 
• 1179348-62-9 1-(4-bromophenyl)-2-(2-dimethyl(oxo)-λ⁶-sulfanylidene)ethan-1-one 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 927825-98-7 [1-(4-bromo-phenyl)-vinyloxy]-triisopropyl-silane 

Downstream Products

• 1034891-24-1 1-(4-cyclopropylphenyl)-2-methoxyethanone 
• 14966-77-9 6-(4-bromo-phenyl)-3,4-diphenyl-2H-pyran-2-one 

Relevant articles and documents

Intermolecular C-O Bond Formation with Alkoxyl Radicals: Photoredox-Catalyzed α-Alkoxylation of Carbonyl Compounds

Due to the high reactivity of alkoxyl (RO·) radicals and their propensity to easily undergo β-scission or Hydrogen Atom Transfer (HAT) reactions, intermolecular alkoxylations involving RO· radicals are barely described. We report herein for the first time the efficient intermolecular trapping of alkoxyl radicals by silyl enol ethers. This photoredox-mediated protocol enables the introduction of both structurally simple and more complex alkoxy groups into a wide range of ketones and amides.

HETEROCYCLIC COMPOUND

A compound represented by the formula (I): wherein each symbol is as described in the SPECIFICATION, or a salt thereof has a PDE2A inhibitory action, and is useful as a prophylactic or therapeutic drug for schizophrenia, Alzheimer's disease and the like.

HETEROCYCLIC COMPOUND

The problem of the present invention is to provide a compound having a PDE2A inhibitory action, and useful as a prophylactic or therapeutic drug for schizophrenia, Alzheimer's disease and the like. The present invention relates to a compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof.