6970-47-4

Basic information

• Product Name: N-[4-(benzylideneamino)butyl]-1-phenyl-methanimine
• CAS NO: 6970-47-4
• Molecular Formula: C₁₈H₂₀N₂
• Molecular Weight: 264.37
• Mol File: 6970-47-4.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 414.4°Cat760mmHg
• Flash Point: 197°C
• Density: 0.96g/cm³
• CAS DataBase Reference: N-[4-(benzylideneamino)butyl]-1-phenyl-methanimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(benzylideneamino)butyl]-1-phenyl-methanimine(6970-47-4)
• EPA Substance Registry System: N-[4-(benzylideneamino)butyl]-1-phenyl-methanimine(6970-47-4)

Safety Data

• Hazardous Substances Data: 6970-47-4(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 110-60-1 1,4-diaminobutane 

Downstream Products

• 16011-97-5 N,N'-dimethyl-1,4-butanediamine 
• 18315-80-5 ethyl α-nitrocinnamate 
• 31991-78-3 uvariadiamide 
• 31719-05-8 N,N'-dibenzylbutane-1,4-diamine 
• 133603-99-3 (2R,3R)-2,3-Diphenyl-[1,4]diazocane 
• 75189-96-7 C₂₀H₂₆N₂⁽²⁺⁾*2CH₃O₄S^(1-) 
• 29867-15-0 N,N'-(butane-1,4-diyl)bis(N-benzylethanamide) 
• 107886-60-2 C₅₁H₅₇N₅O₄ 
• 107886-64-6 C₅₁H₅₇N₅O₄ 
• 107886-62-4 N,N'-dibenzyl-N-(4-phthalimidobutyl)-1,4-diaminobutane 
• 107886-63-5 N,N'-dibenzyl-N-(3-phthalimidopropyl)-1,4-diaminobutane 
• 940295-90-9 N,N'-butane-1,4-diylbis[N-benzyl-P,P-diphenyl(phosphinic amide)] 
• 1311508-42-5 C₂₆H₃₂N₂O₆ 

Relevant articles and documents

A minimalistic approach to develop new anti-apicomplexa polyamines analogs

The development of new chemical entities against the major diseases caused by parasites is highly desired. A library of thirty diamines analogs following a minimalist approach and supported by chemoinformatics tools have been prepared and evaluated agains

Photophysical properties of di-Schiff bases: Evaluating the synergistic effect of non-covalent interactions and alkyl spacers in enhanced emissions of solids

Photophysical properties of di-Schiff base compounds in the solution and solid states are explored. The di-Schiff bases with alkyl spacers (ethyl, butyl and hexyl) showed enhanced light emitting properties in the solid state, while quenching was observed for di-Schiff bases with a hydrazine spacer. The photoluminescence spectra and the crystal structure were compared with bis-pyridyl-ethyl-di-imine and bis-pyridyl-butyl-di-imine. The crystal structure analysis of the compounds rationalizes the observed results. The concentration dependent 1H-NMR and NOESY spectra showed the aggregation behaviour of the compounds.

Design, synthesis and biological activity of peptidomimetic analogs of insect allatostatins

Allatostatins (ASTs) comprise a family of insect neuropeptides isolated from cockroaches and found to inhibit the production of juvenile hormone (JH) by the corpora allata (CA). For this reason, the ASTs can be regarded as possible IGR candidates for pest control. Six peptidomimetic analogs according to the C-terminal pentapeptide of ASTs were prepared by solid-phase organic synthetic methods in an attempt to obtain new simple substitution agents. Assays of inhibition of JH biosynthesis in vitro by corpora allata from the cockroach Diploptera punctata showed that the activity of analog I (IC50: 0.09 μM) was more active than that of the C-terminal pentapeptide (Tyr-Xaa-Phe-Gly-Leu-NH2, IC50: 0.13 μM) it mimicked and the activity of the analog II (IC50: 0.13 μM) proved roughly equivalent to the C-terminal pentapeptide. The results indicate that a new simple mimicry for Tyr-Xaa-Phe-Gly has been discovered; analog I may be a novel compound candidate for potential IGRs. This study will be useful for the design of new AST analogs for insect management.