3910-55-2

Basic information

• Product Name: 1-Butanamine, N-[(4-methoxyphenyl)methylene]-
• CAS NO: 3910-55-2
• Molecular Formula: C12H17NO
• Molecular Weight: 191.273
• Mol File: 3910-55-2.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: 1-Butanamine, N-[(4-methoxyphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanamine, N-[(4-methoxyphenyl)methylene]-(3910-55-2)
• EPA Substance Registry System: 1-Butanamine, N-[(4-methoxyphenyl)methylene]-(3910-55-2)

Safety Data

• Hazardous Substances Data: 3910-55-2(Hazardous Substances Data)

Usage

Functional Groups

Butanamine moiety, substituted benzaldehyde group

Structure

A butanamine group with a benzaldehyde group attached to the nitrogen atom

Usage

Building block in organic synthesis

Applications

Production of pharmaceuticals, agrochemicals, and other fine chemicals

Reactivity

Can undergo a variety of chemical reactions

Reactions

Formation of imines, reductive amination, and other transformations

Importance

Valuable tool in organic chemistry

Versatility

Key component in the synthesis of diverse compounds

Industrial and Commercial Applications

Potential use in various industries due to its reactivity and versatility

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 109-73-9 N-butylamine 
• 7332-00-5 n-butylazide 
• 3246-78-4 N-(4-methoxybenzylidene)-4-methylaniline 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 874-90-8 4-methoxybenzonitrile 
• 2393-23-9 4-methoxy-benzylamine 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 88818-49-9 1-(4-Methoxyphenyl)-2-nitro-1-buten-3-one 
• 54209-32-4 3-butyl-2,6-bis-(4-methoxy-phenyl)-2,3-dihydro-[1,3,5]oxadiazine-4-thione 
• 3910-58-5 N-(4-methoxybenzyl)butan-1-amine 
• 4589-09-7 meso-1,2-Bis(4-methoxyphenyl)-N,N'-dibutylethylendiamin 
• 65908-33-0 6-methoxy-2,3-diphenyl-1H-inden-1-one 
• 105202-53-7 3-(4-methoxyphenyl)-2-nitro-1-phenyl-2-propen-1-one 
• 127143-28-6 1-(2-chloro-2-nitroethenyl)-4-methoxybenzene 
• 22013-86-1 1-(2-bromo-2-nitrovinyl)-4-methoxybenzene 
• 141-05-9 Diethyl maleate 
• 1019490-45-9 N-butyl-N-[1-(4-methoxyphenyl)propyl]amine 
• 3246-78-4 N-(4-methoxybenzylidene)-4-methylaniline 
• 109-73-9 N-butylamine 

Relevant articles and documents

[2]Pseudorotaxanes based on naphtho-21-crown-7 and secondary dialkylammonium salts: Remarkably improved association constants among four threaded structures

This research article is focused on the recognition interaction of a new host naphtho-21-crown-7 and four secondary dialkylammonium salts. In acetone, they can form 1:1 host-guest complexes which belong to slow-exchange systems. We also found the differen

Tunable Synthesis of α-Amino Boronic Esters from Available Aldehydes and Amines through Sequential One-Pot Dehydration and Copper-Catalyzed Borylacylation

Copper-catalyzed multicomponent borylacylation of imines with acid chlorides and bis(pinacolato)diboron was developed for the preparation of synthetically useful and pharmacologically relevant α-amino boronic acid derivatives. Starting from a range of acid chlorides and imines with aryl, heteroaryl, and alkyl substituents, most of these ligand-free reactions proceeded smoothly at room temperature in moderate to good yields. Furthermore, a facile and convenient one-pot, multistep access to the direct synthesis of α-amino boronic acid derivatives from available aldehydes and amines was also developed.

Synthesis of Secondary Aldimines from the Hydrogenative Cross-Coupling of Nitriles and Amines over Al2O3-Supported Ni Catalysts

A heterogeneous Ni catalyst was discovered to be active in the synthesis of secondary cross-imines via hydrogenative coupling of nitriles and amines. The mesoporous Al2O3-supported Ni nanoparticles (abbreviated as Ni/m-Al2O3-600, where 600 represents the reduction temperature) were active in hydrogenative coupling of nitriles and amines reaction at 80 °C and 1 bar H2, affording corresponding cross-imines with yields in the range 64.1-98.1%. Density functional theory calculations reveal the hydrogenation of benzonitrile (PhCN) to benzylamine (PhCH2NH2) has higher activation energy than that for hydrogenative cross-coupling of PhCN and RNH2 on the Ni/m-Al2O3-600 catalyst, suggesting the latter reaction is more favorable. The theoretical calculations are in good agreement with our experimental results.