1032080-61-7

Basic information

• Product Name: [1-(3-Chloro-phenyl)-meth-(E)-ylidene]-propyl-amine
• Synonyms: [1-(3-Chloro-phenyl)-meth-(E)-ylidene]-propyl-amine
• CAS NO: 1032080-61-7
• Molecular Weight: 181.665
• Mol File: 1032080-61-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: [1-(3-Chloro-phenyl)-meth-(E)-ylidene]-propyl-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-(3-Chloro-phenyl)-meth-(E)-ylidene]-propyl-amine(1032080-61-7)
• EPA Substance Registry System: [1-(3-Chloro-phenyl)-meth-(E)-ylidene]-propyl-amine(1032080-61-7)

Safety Data

• Hazardous Substances Data: 1032080-61-7(Hazardous Substances Data)

Upstream product

• 107-10-8 propylamine 
• 587-04-2 m-Chlorobenzaldehyde 

Downstream Products

• 39190-98-2 N-(3-chlorobenzyl)propylamine 
• 1262325-33-6 4-(3-chlorobenzylidene)-2-methyl-1-propyl-1H-imidazol-5(4H)-one 
• 1193433-99-6 (E)-5-(3-chlorophenyl)-4-(1-cyclopentenyl)-5-(propylamino)pent-3-en-1-ol 
• 1193433-73-6 (E)-5-(3-chlorophenyl)-5-(propylamino)-4-(1-(triisopropylsilyl)-1H-indol-3-yl)pent-3-en-1-ol 
• 1193433-72-5 (E)-5-(3-chlorophenyl)-5-(propylamino)-4-(1-(triisopropylsilyl)-1H-pyrrol-3-yl)pent-3-en-1-ol 
• 1193433-71-4 (E)-5-(3-chlorophenyl)-4-(furan-3-yl)-5-(propylamino)pent-3-en-1-ol 
• 1193433-70-3 (E)-5-(3-chlorophenyl)-5-(propylamino)-4-(thiophen-3-yl)pent-3-en-1-ol 
• 1193433-69-0 (E)-4-(benzo[d][1,3]dioxol-5-yl)-5-(3-chlorophenyl)-5-(propylamino)pent-3-en-1-ol 
• 1193433-68-9 (E)-4-(3-bromophenyl)-5-(3-chlorophenyl)-5-(propylamino)pent-3-en-1-ol 
• 1193433-67-8 (E)-5-(3-chlorophenyl)-4-phenyl-5-(propylamino)pent-3-en-1-ol 

Relevant articles and documents

A latent reaction in a model GFP chromophore revealed upon confinement: Photohydroxylation of ortho -halo benzylidene-3-methylimidazolidiones via an electrocylization process

Excited state behavior of halogen substituted model GFP chromophores was investigated in an acetonitrile solution and in a confined environment provided by an octa acid capsule in water. Of the ortho, meta, and para halogen substituted GFP chromophores on

Preparation of benzolactams by Pd(OAC)2-catalyzed direct aromatic carbonylation

We developed a new method for Pd(II)-catalyzed direct aromatic carbonylation in a phosphine-free catalytic system using Pd(OAc)2 and Cu(OAc)2 in an atmosphere of CO gas containing air. The carbonylation proceeded with ortho-palladation, inducing a remarkable site selectivity to afford a variety of five- or six-membered benzolactams from secondary ω-arylalkylamines, such as N-alkylbenzylamines or N-alkylphenethylamines. Copyright

Benzylamines: Synthesis and evaluation of antimycobacterial properties

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.