CAS 1734-79-8
:4-Nitrocinnamaldeído
- (E)-3-(4-nitrophenyl)prop-2-enal
- (Z)-3-(4-nitrophenyl)prop-2-enal
- 2-Propenal, 3-(4-nitrophenyl)-
- 3-(4-Nitrophenyl)-2-propenal
- 3-(4-Nitrophenyl)acrolein
- 3-(4-Nitrophenyl)acrylaldehyde
- 4-Nitrocinnamaldahyde
- 4-Nitrocinnamic aldehyde
- Brn 1565424
- Ccris 3774
- Cinnamaldehyde, p-nitro-
- Nsc 1318
- p-Nitrocinnamaldehyde
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(E)-4-Nitrocinnamaldehyde
CAS:Fórmula:C9H7NO3Pureza:>98.0%(GC)Cor e Forma:Light yellow to Brown to Dark green powder to crystalPeso molecular:177.163-(4-Nitrophenyl);acrylaldehyde
CAS:Fórmula:C9H7NO3Pureza:97%Cor e Forma:SolidPeso molecular:177.15683-(4-Nitrophenyl)acrylaldehyde
CAS:3-(4-Nitrophenyl)acrylaldehydePureza:97%Peso molecular:177.16g/mol4-Nitrocinnamaldehyde
CAS:4-Nitrocinnamaldehyde is a diazonium salt that is used as an efficient method for the synthesis of nitro compounds. Nitro compounds are used in the production of explosives, insecticides, and herbicides. 4-Nitrocinnamaldehyde reacts with hydrochloric acid to produce trifluoroacetic acid, which is then reacted with an organic compound to produce a nitro compound. This reaction has been shown to be irreversible and not sensitive to functional groups. 4-Nitrocinnamaldehyde binds to the enzyme cytochrome P450 reductase, inhibiting its function. The binding of 4-nitrocinnamaldehyde to enzymes such as pyruvate kinase and acetylcholinesterase has also been observed in binding experiments.
Fórmula:C9H7NO3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:177.16 g/mol4-Nitrocinnamaldehyde, predominantly trans, 98%
CAS:Doebner-Miller reaction the 4- nitrocinnamaldehyde and 2-methylaniline in concentrated HC1 give the corresponding 8-methyl-2-phenylquinoline (3: R = 4'-N02) directly. The asymmetric Friedel-Crafts-type alkylation in aqueous media reaction of 4-Nitrocinnamaldehydr with N-methyl indole using trifluoro
Fórmula:C9H7NO3Pureza:98%Cor e Forma:White to yellow to orange, PowderPeso molecular:177.16





