143278-21-1

Basic information

• Product Name: Ethanone, 1-(4-ethylphenyl)-2-iodo-
• CAS NO: 143278-21-1
• Molecular Formula: C10H11IO
• Molecular Weight: 274.101
• Mol File: 143278-21-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-ethylphenyl)-2-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-ethylphenyl)-2-iodo-(143278-21-1)
• EPA Substance Registry System: Ethanone, 1-(4-ethylphenyl)-2-iodo-(143278-21-1)

Safety Data

• Hazardous Substances Data: 143278-21-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(4-ethylphenyl)-2-iodo- is a chemical compound that belongs to the ketone functional group, featuring an ethylphenyl group and an iodine atom. It is commonly used in organic synthesis as a building block for creating more complex molecules. This chemical's structure allows for it to participate in a variety of reactions, making it a versatile reagent in the laboratory. However, due to its potentially hazardous nature as an iodinated compound, proper safety measures must be taken when handling and storing this substance.

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Relevant articles and documents

AuIII-Catalyzed Formation of α-Halomethyl Ketones from Terminal Alkynes

A AuIII-catalyzed synthesis of α-halomethyl ketones from terminal alkynes was developed. This approach features excellent functional group compatibility and good yields for both aromatic and aliphatic terminal alkynes. The resulting α-halomethyl ketones were used to prepare heterocyclic indolizine structures. The plausible mechanism of the one-pot reaction is proposed.

Preparation of Aromatic Iodoacetyl Derivatives by Direct Iodination with a Potassium Iodide-Potassium Iodate-Sulfuric Acid System

The reaction of aromatic acetyl derivatives with potassium iodide and potassium iodate in acetic acid in the presence of sulfuric acid at room temperature gave iodoacetyl derivatives in good yields.