79421-41-3

Usage

General Description

1-(4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)phenyl)ethanone is a chemical compound with a complex structure that includes a 1,4-dioxa-8-azaspiro[4.5]decan-8-yl group attached to a phenyl ring, which in turn is attached to an ethanone molecule. 1-(4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)phenyl)ethanone is likely to have a variety of potential uses and applications in various fields, given its unique structure and potential reactivity. However, further research and analysis would be needed to fully understand the properties and potential uses of this chemical. Additionally, given its complex structure, precautions should be taken when handling and working with 1-(4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)phenyl)ethanone to ensure safety and proper handling.

Upstream product

• 177-11-7 4,4-ethylenedioxy-piperidine 
• 149104-90-5 4-acetylphenylboronic acid 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 340756-77-6 [4-(4-oxopiperidin-1-yl)phenyl]acetic acid 
• 79421-48-0 1-(4-Acetylphenyl)piperidin-4-on 

Relevant academic research and scientific papers

Structure of 8-(4-Acetylphenyl)-1,4-dioxa-8-azaspirodecane: a New Potential Nonlinear Optical Material

The crystals of the title compound (APDA), C15H19NO3, which belong to a non-centrosymmetric space group Pna21, show significant second harmonic generation efficiency and no absorption for light with a wavelength longer than 400 nm.

Ligand- and Base-Free Copper(II)-Catalyzed C-N Bond Formation: Cross-Coupling Reactions of Organoboron Compounds with Aliphatic Amines and Anilines

(Equation presented) A ligandless and base-free Cu-catalyzed protocol for the cross-coupling of arylboronic acids and potassium aryltrifluoroborate salts with primary and secondary aliphatic amines and anilines is described. The process utilizes catalytic copper(II) acetate monohydrate and 4 A molecular sieves in dichloromethane at slightly elevated temperatures under an atmosphere of oxygen. A broad range of functional groups are tolerated on both of the cross-coupling partners.