7173-86-6

Basic information

• Product Name: N-[(E)-(4-chlorophenyl)methylidene]butan-1-amine
• Synonyms: p-chlorobenzylidene-butyl-amine
• CAS NO: 7173-86-6
• Molecular Formula: C₁₁H₁₄ClN
• Molecular Weight: 195.6886
• Mol File: 7173-86-6.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 272.9°C at 760 mmHg
• Flash Point: 118.8°C
• Density: 1g/cm³
• Vapor Pressure: 0.0099mmHg at 25°C
• Refractive Index: 1.51
• CAS DataBase Reference: N-[(E)-(4-chlorophenyl)methylidene]butan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(E)-(4-chlorophenyl)methylidene]butan-1-amine(7173-86-6)
• EPA Substance Registry System: N-[(E)-(4-chlorophenyl)methylidene]butan-1-amine(7173-86-6)

Safety Data

• Hazardous Substances Data: 7173-86-6(Hazardous Substances Data)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 109-73-9 N-butylamine 
• 104-88-1 4-chlorobenzaldehyde 
• 706-07-0 1-chloro-4-(2-nitrovinyl)benzene 
• 873-76-7 para-Chlorobenzyl alcohol 
• 5577-66-2 trimethyl(butyl-amino)silane 

Downstream Products

• 16183-32-7 N-(4-chlorobenzyl)butan-1-amine 
• 1361411-97-3 diethyl ((butylamino)(4-chlorophenyl)methyl)phosphonate 
• 1417526-40-9 1-n-butyl-5-(4-chlorophenyl)-1H-imidazole 
• 1417526-41-0 1-n-butyl-5-(4-chlorophenyl)-1H-imidazole-2-carbaldehyde 
• 1391156-02-7 diethyl 2-(4-chlorophenyl)-1,1-difluoro-2-butylaminoethylphosphonate 
• 91634-40-1 4-(4-chloro-phenyl)-isoxazole-3,5-dicarboxylic acid 
• 108934-21-0 4-(2'-methylphenyl)benzaldehyde 
• 3218-36-8 4-Phenylbenzaldehyde 
• 1200-14-2 4-(n-butyl)benzaldehyde 
• 27634-89-5 4-cyclohexylbenzaldehyde 
• 101495-61-8 1-chloro-4-(2-chloro-2-nitroethenyl)benzene 
• 94436-54-1 4-(4-chloro-phenyl)-isoxazole-3,5-dicarboxylic acid bis-butylamide 
• 60859-80-5 ethyl (Z)-3-(4-chlorophenyl)-2-nitropropenoate 

Relevant articles and documents

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.

Integrative Theory/Experiment-Driven Exploration of a Multicomponent Reaction towards Imidazoline-2-(thi)ones

Predicting reactivity in multicomponent reactions (MCRs) is extremely difficult. These reactions proceed by multiple pathways and are inherently associated with a potentially large variation of reactants and functional groups. To date, theoretical chemist

Direct synthesis of imines by 9-azabicyclo-[3,3,1]nonan-N-oxyl/KOH-catalyzed aerobic oxidative coupling of alcohols and amines

A simple and efficient method for preparation of imines by the oxidative coupling of benzyl alcohols with aromatic amines or aliphatic amines was developed. The reaction was catalyzed by 9-azabicyclo[3.3.1]nonan-N-oxyl (ABNO)/KOH with air as the economic and green oxidant. Under the optimal reaction conditions, a variety of imines were obtained in 80%-96% isolated yields.