856936-55-5

Usage

Uses

Used in Pharmaceutical Industry:
Tert-Butyl 4-(4-Methoxybenzoyl)piperidine-1-carboxylate is used as a key intermediate in the synthesis of new drugs and active pharmaceutical ingredients. Its methoxybenzoyl group contributes to the development of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Tert-Butyl 4-(4-Methoxybenzoyl)piperidine-1-carboxylate is utilized as a precursor for the creation of new agrochemicals, potentially leading to advancements in crop protection and pest management.
Used in Organic Chemistry Research:
tert-Butyl 4-(4-Methoxybenzoyl)piperidine-1-carboxylate serves as a versatile building block in organic chemistry, enabling the synthesis of a wide range of organic compounds for various applications, including the development of new materials and chemical processes.

Upstream product

• 1046478-89-0 tert-butyl 4-(p-tolylsulfonylhydrazono)-piperidine-1-carboxylate 
• 123-11-5 4-methoxy-benzaldehyde 
• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 139290-70-3 tert-butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate 
• 137076-22-3 tert butyl 4-formylpiperidine-1-carboxylate 

Downstream Products

• 76362-12-4 4-(4-methoxybenzoyl)-piperidine 

Relevant academic research and scientific papers

Aromatic cycloamines derivative and application in multi-target antidepressant medicine

The invention discloses an aromatic cycloamines derivative and an application in multi-target antidepressant medicine. The aromatic cycloamines derivative has inhibitory activity on 5-HT reuptake, NEreuptake and DA reuptake, is a novel compound of a 5-HT/

ALPHA-SYNUCLEIN LIGANDS

The present invention generally relates to various compounds that are useful as α-synuclein ligands. The invention further relates to methods of using these compounds and their radiolabeled analogs for the detection of synucleinopathies, including Parkinson's disease (PD).

Direct Aldehyde C-H Arylation and Alkylation via the Combination of Nickel, Hydrogen Atom Transfer, and Photoredox Catalysis

A mechanism that enables direct aldehyde C-H functionalization has been achieved via the synergistic merger of photoredox, nickel, and hydrogen atom transfer catalysis. This mild, operationally simple protocol transforms a wide variety of commercially available aldehydes, along with aryl or alkyl bromides, into the corresponding ketones in excellent yield. This C-H abstraction coupling technology has been successfully applied to the expedient synthesis of the medicinal agent haloperidol.

Preparation of unsymmetrical ketones from tosylhydrazones and aromatic aldehydes via formyl C-H bond insertion

Preparation of ketones by insertion of diazo compounds into the formyl C-H bond of an aldehyde is an attractive procedure, but use of structurally diverse diazo compounds is hampered by preparation and safety issues. A convenient procedure for the synthesis of unsymmetrical ketones from bench-stable tosylhydrazones and aryl aldehydes is reported. The procedure can be performed in one pot from the parent carbonyl compound and needs only a base, with no additional promoters being required.