22210-79-3

Basic information

• Product Name: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-dimethyl-
• CAS NO: 22210-79-3
• Molecular Formula: C18H22N2
• Molecular Weight: 266.386
• Mol File: 22210-79-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-dimethyl-(22210-79-3)
• EPA Substance Registry System: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-dimethyl-(22210-79-3)

Safety Data

• Hazardous Substances Data: 22210-79-3(Hazardous Substances Data)

Upstream product

• 100-10-7 4-dimethylamino-benzaldehyde 
• 7647-01-0 hydrogenchloride 
• 50-00-0 formaldehyd 
• 22525-43-5 trans-4′-(N,N′-dimethylamino)-4-aminostilbene 
• 78-08-0 Triethoxyvinylsilane 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 186581-53-3 diazomethane 
• 142581-66-6 (N(CH₃)2)C₆H₄CHC₆H₄(N(CH₃)2)⁽¹⁺⁾*CF₃SO₃^(1-) = CF₃SO₃{(N(CH₃)2)C₆H₄CHC₆H₄(N(CH₃)2)} 
• 18107-18-1 diazomethyl-trimethyl-silane 

Relevant articles and documents

Relaxation pathways in photoexcited electron-rich stilbenes (D-D stilbenes) as compared to D-A stilbenes

Spectra and shifts, fluorescence quantum yields and lifetimes of 4,4'-dimethylaminostilbene (DDS) and the bridged derivatives DDS-B15 and DDS-B24 were measured as a function of solvent polarity and temperature. The behavior of DDS and DDS-B15 is interpret

Reductive coupling of carbonyl compounds promoted by cobalt or titanium nanoparticles

The reaction of a series of aldehydes and ketones with readily prepared cobalt or titanium nanoparticles, under mild reaction conditions, led to the obtention of different reductive dimerization products depending on the nature of the transition metal used. Cobalt nanoparticles (CoNPs) allowed the selective transformation of the starting carbonyl compounds into vicinal diols, whereas the reaction promoted by titanium nanoparticles (TiNPs) led to the formation of the corresponding alkenes. In this last case, the use of trimethylsilyl chloride (TMSCl) as additive, at 0 °C, also allowed the obtention of vicinal diols after acidic aqueous work-up. ARKAT-USA, Inc.

Spectroscopic Correlations between Supermolecules and Molecules. Anatomy of the Ion-Modulated Electronic Properties of the Nitrogen Donor in Monoazacrown-Derived Intrinsic Fluoroionophores

The synthesis, absorption and emission spectra, fluorescence quantum yields, and fluorescence lifetimes of three compound series of trans-4,4′-disubstituted aminostilbenes (1-3) are reported. The chromo-/fluoroionophoric behavior of the monoaza-15-crown-5