82363-30-2

Basic information

• Product Name: (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE
• Synonyms: (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE;N-(3,4-dimethoxybenzyl)aniline
• CAS NO: 82363-30-2
• Molecular Formula: C₁₅H₁₇NO₂
• Molecular Weight: 243.3
• Mol File: 82363-30-2.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE(82363-30-2)
• EPA Substance Registry System: (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE(82363-30-2)

Safety Data

• Hazardous Substances Data: 82363-30-2(Hazardous Substances Data)

Usage

Description

(3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE is a chemical compound with the molecular formula C15H17NO2. It is a derivative of benzylamine and contains two methoxy groups on the benzene ring. (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE is known for its unique chemical structure and reactivity, making it a valuable component in the synthesis of various pharmaceuticals and organic compounds.

Uses

Used in Pharmaceutical Synthesis:
(3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE is used as a building block in the production of complex organic molecules, particularly in the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in creating a wide range of medicinal compounds.
Used in Organic Compound Synthesis:
In the field of organic chemistry, (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE is used as a reagent in chemical reactions. Its reactivity contributes to the formation of various organic compounds, making it a versatile tool for chemists.
Used in Medicinal Chemistry and Drug Discovery:
(3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE also has potential applications in the field of medicinal chemistry and drug discovery. As a precursor in the synthesis of potential drug candidates, it plays a crucial role in the development of new therapeutic agents.
Used in Chemical Reactions:
Furthermore, (3,4-DIMETHOXY-BENZYL)-PHENYL-AMINE is utilized as a reagent in various chemical reactions, facilitating the synthesis of a broad spectrum of chemical products, which can be applied across different industries.

Upstream product

• 27895-67-6 N-(3,4-dimethoxybenzylidene)aniline 
• 114468-29-0 (E)-1-(3,4-dimethoxyphenyl)-N-phenylmethanimine 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 62-53-3 aniline 
• 98-95-3 nitrobenzene 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 5763-61-1 3,4-dimethoxybenzylamine 
• 98-80-6 phenylboronic acid 
• 106-49-0 p-toluidine 

Downstream Products

• 1295581-88-2 N-benzyl-N-(3,4-dimethoxybenzyl)aniline 
• 1295581-89-3 N-(3,4-dimethoxybenzyl)-N-phenethylaniline 
• 27895-67-6 N-(3,4-dimethoxybenzylidene)aniline 

Relevant articles and documents

Boron-containing capsaicinoids

This study reports on the preparation of eight new boron-containing capsaicinoids bearing long aliphatic chains, as an expansion of our previous studies to include tertiary amide derivatives into our substrate scope. Our boron-moiety, a pinacolboronate es

Ru(II)-NHC catalysed N-Alkylation of amines with alcohols under solvent-free conditions

The reaction of [RuCl2(p-cymene)]2 with in situ prepared Ag-N-heterocyclic carbene (NHC) complexes yields a series of [RuCl2(p-cymene)(NHC)] complexes (2). All of the complexes have been characterised by elemental analysis, and 1H NMR and 13C NMR spectroscopies. These complexes have been tested for the N-alkylation of aromatic amines with arylmethyl alcohols under neat conditions in the presence of KOtBu at 120 °C. Compounds (2) are stable and have high catalytic/selective activity for the N-alkylation reactions of primary amines to afford secondary amines.

Direct electrochemical reductive amination between aldehydes and amines with a H/D-donor solvent

A novel electrochemical synthesis protocol has been achieved for reductive amination between aldehydes and amines in undivided cells at room temperature. Under metal-free and external-reductant-free electrolysis conditions, various important secondary amine products are obtained in moderate-to-high yields. Deuterium-labeling experiments have demonstrated that low-toxicity DMSO acts both as a solvent and a H-donor in the reaction. On this basis, various deuterium-labeled products with good-to-excellent D-incorporation have been synthesized by using DMSO-d6 as a solvent. Furthermore, a molecule with GR-antagonistic activity has been synthesized through further sulfonylation.