5267-46-9

Usage

Uses

Used in Pharmaceutical Industry:
C-(4-Methoxy-phenyl)-C-phenyl-methyl-ammonium chloride is used as a phase-transfer catalyst for facilitating organic synthesis reactions in the pharmaceutical industry. Its ability to transfer reactants between phases makes it a valuable tool in the production of various drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, C-(4-Methoxy-phenyl)-C-phenyl-methyl-ammonium chloride serves as a phase-transfer catalyst, aiding in the synthesis of various agrochemical products. This includes the production of pesticides, herbicides, and other substances used in agriculture to protect crops and enhance yields.
Used in Dyes and Pigments Production:
C-(4-Methoxy-phenyl)-C-phenyl-methyl-ammonium chloride is utilized as a phase-transfer catalyst in the production of dyes and pigments. Its role in organic synthesis allows for the creation of a wide range of colors and hues used in various industries, such as textiles, plastics, and printing.
Used as an Antibacterial and Antifungal Agent:
C-(4-Methoxy-phenyl)-C-phenyl-methyl-ammonium chloride has been studied for its potential use as an antibacterial and antifungal agent. Its properties make it a candidate for further research and development in the field of antimicrobial agents, which could be applied in various settings, including healthcare and sanitation.

InChI:InChI=1/C14H15NO/c1-16-13-9-7-12(8-10-13)14(15)11-5-3-2-4-6-11/h2-10,14H,15H2,1H3

Upstream product

• 69939-39-5 N-(diphenylmethylene)-1-(p-methoxyphenyl)-1-phenylmethanamine 
• 100-46-9 benzylamine 
• 108-86-1 bromobenzene 
• 78999-89-0 N-(diphenylmethylene)-1-(4-methoxyphenyl)methanamine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 7699-79-8 benzhydrylidene-benzyl-amine 
• 180399-97-7 [1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-phosphoramidic acid diethyl ester 
• 611-94-9 4-Methoxybenzophenone 

Relevant academic research and scientific papers

Synthesis of diarylmethylamines via palladium-catalyzed regioselective arylation of 1,1,3-triaryl-2-azaallyl anions

Diarylmethylamines are of great interest due to their prevalence in pharmaceutical chemistry. As a result, new methods for their synthesis are in demand. Herein, we report a versatile protocol for the synthesis of diarylmethylamine derivatives involving palladium-catalyzed arylation of in situ generated 2-azaallyl anion intermediates. The 2-azaallyl anions are generated by reversible deprotonation of readily available aldimine and ketimine precursors. Importantly, the arylated aldimine and ketimine products do not undergo isomerization under the reaction conditions. Scale-up of the arylation and hydrolysis of the resulting products to furnish diarylmethylamines were also successfully performed. This journal is the Partner Organisations 2014.

Synthesis of α-arylalkylamines by addition of Grignard reagents to N- (diethoxyphosphoryl)aldimines

Addition of organomagnesium bromides to N-(diethoxyphosphoryl) aldimines 1 carded out in tetrahydrofuran at 20-25°C affords diethyl N-alkyl- phosphoramidates 2a-w in high yields and spectroscopic purity. Deprotection of the latent amino groups in 2 results in the formation of α-arylalkylamine hydrochlorides 3a-w.