Diazene,1-(4-nitrophenyl)-2-phenyl-
Diazene,1-(4-nitrophenyl)-2-phenyl- structure
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Common Name | Diazene,1-(4-nitrophenyl)-2-phenyl- | ||
|---|---|---|---|---|
| CAS Number | 2491-52-3 | Molecular Weight | 227.21900 | |
| Density | 1.23g/cm3 | Boiling Point | 392.9ºC at 760mmHg | |
| Molecular Formula | C12H9N3O2 | Melting Point | 132-134ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 191.4ºC | |
| Symbol |
GHS07, GHS08 |
Signal Word | Warning | |
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Mutagenicity of 4-aminoazobenzene, N-hydroxy-4-aminoazobenzene, 4-nitrosoazobenzene, 4-nitroazobenzene, and their ring methoxylated derivatives on Salmonella.
Gann 72(6) , 921-9, (1981) The mutagenicities of 4-aminoazobenzene (AAB), N-hydroxy-4-aminoazobenzene, 4-nitroazobenzene, and their 2-, 3-, 4'-methoxyl and 2,5-dimethoxyl derivatives, and 2- and 3-methoxy-4-nitrosoazobenzene were examined on Salmonella typhimurium TA98 and TA100. The a... |
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Determination of the structure and orientation of organic molecules tethered to flat graphitic carbon by ATR-FT-IR and Raman spectroscopy.
Anal. Chem. 78(9) , 3104-12, (2006) Mono- and multilayers of nitroazobenzene (NAB), azobenzene (AB), nitrobiphenyl (NBP), biphenyl (BP), and fluorene (FL) were covalently bonded to flat pyrolyzed photoresist films (PPF) by electrochemical reduction of their diazonium derivatives. The structure ... |
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Resonance Raman spectroscopy and quantum-chemical calculations of push-pull molecules: 4-hydroxy-4'-nitroazobenzene and its anion.
J. Phys. Chem. A 111(51) , 13452-6, (2007) The deprotonation of the push-pull molecule 4-hydroxy-4'-nitroazobenzene leads to a substantial variation in the charge distribution over the donor and acceptor moieties in the D-pi-azo-pi-A system. The extra charge stabilizes the excited state, leading to a ... |
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Synthesis, spectroscopy and photochemistry of nitro-azobenzene dyes bearing benzophenone parts.
J. Fluoresc. 19(3) , 533-44, (2009) Novel nitro-azobenzene dyes bearing one or two benzophenone branches were proposed and synthesized to improve their photophysical and photochemical properties. The new dyes exhibited double UV/visible bands, and they displayed weak fluorescence emission as ex... |