64128-27-4

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(4-butylphenyl)-, oxime is used as a pharmaceutical intermediate for the synthesis of various drugs. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of new therapeutic agents.
Used in Food Additives Industry:
Ethanone, 1-(4-butylphenyl)-, oxime is used as a food additive due to its antioxidant properties. It helps in preserving the quality and extending the shelf life of food products by preventing oxidation and spoilage.
Used in Fragrance Industry:
Ethanone, 1-(4-butylphenyl)-, oxime is used as a fragrance ingredient in the perfumery and cosmetics industry. Its unique scent profile contributes to the creation of various fragrances and perfumes.
Used in Organic Chemistry Research:
Ethanone, 1-(4-butylphenyl)-, oxime serves as a reagent in organic chemistry for the transformation of ketones to oximes. It is utilized in various research applications to study the properties and reactions of oxime derivatives.

Upstream product

• 37920-25-5 1-(4-butylphenyl)ethanone 

Downstream Products

• 1415585-94-2 N-(1-(4-butylphenyl)vinyl)acetamide 
• 64128-37-6 C₂₅H₃₃NO₃ 
• 64128-44-5 C₂₆H₃₅NO₂ 

Relevant academic research and scientific papers

Iron-Catalyzed Synthesis of 2H-Imidazoles from Oxime Acetates and Vinyl Azides under Redox-Neutral Conditions

A novel and versatile method for the synthesis of 2H-imidazoles via iron-catalyzed [3 + 2] annulation from readily available oxime acetates with vinyl azides has been developed. This denitrogenative process involved N-O/N-N bond cleavages and two C-N bond formations to furnish 2,4-substituted 2H-imidazoles. This protocol was performed under mild reaction conditions and needed no additives or ligands. Furthermore, this is a green reaction involving oxime acetate as internal oxidant, acetic acid, and nitrogen as byproducts.

Palladium-Catalyzed C-H Functionalization of Aromatic Oximes: A Strategy for the Synthesis of Isoquinolines

An efficient strategy for synthesis of isoquinolines via Pd(II)-catalyzed cyclization reaction of oximes with vinyl azides or homocoupling of oximes is reported. Oximes could serve as a directing group and an internal oxidant in the transformation. This reaction features good functional group tolerance and provides a useful protocol for the synthesis of different kinds of isoquinolines under mild conditions. Some control experiments and 15N isotope labeling experiments were conducted for the mechanistic research. (Chemical Equation Presented).