(E)-4-Nitrocinnamaldehyde

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Names

[ CAS No. ]:
49678-08-2

[ Name ]:
(E)-4-Nitrocinnamaldehyde

[Synonym ]:
MFCD00007379
4-Nitro-benzoldiazohydroxid
4-Nitro-benzol-isodiazotat
Benzenamine,4-nitro-N-nitroso
p-nitro-cinnamaldehyde
trans-4-nitrocinnamaldehyde
trans-4-nitro-cinnamic aldehyde
4-Nitro-benzol-anti-diazotat
EINECS 217-076-8

Chemical & Physical Properties

[ Melting Point ]:
140-143ºC(lit.)

[ Molecular Formula ]:
C9H7NO3

[ Molecular Weight ]:
177.15700

[ Exact Mass ]:
177.04300

[ PSA ]:
62.89000

[ LogP ]:
2.33010

[ Storage condition ]:
0-6°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
36/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
GD6650000

Synthetic Route

Precursor & DownStream

Precursor

  • 4-nitrocinnamyl alcohol
  • 1-Iodo-4-nitrobenzene
  • 3,3-Diethoxy-1-propene
  • 4-Nitrobenzaldehyde
  • ch3cho
  • 1-Bromo-4-nitrobenzene
  • acrolein
  • AZELASTINEHYDROCHLORIDEE
  • (E)-N-methoxy-N-methyl-4-nitrocinnamamide
  • triphenylarsonium salt of bromoacetaldehyde

DownStream

  • [(2S,3S)-3-(4-nitrophenyl)oxiran-2-yl]methanol
  • 4-[(E)-2-(1H-BENZOIMIDAZOL-2-YL)VINYL]PHENYLAMINE
  • 3-(4-nitrophenyl)prop-2-enamide
  • AZELASTINEHYDROCHLORIDEE
  • 4-nitrocinnamyl alcohol

Articles

Reactivity at the substrate activation site of yeast pyruvate decarboxylase: inhibition by distortion of domain interactions.

Biochemistry 37(5) , 1245-55, (1998)

The residue C221 on pyruvate decarboxylase (EC. 4.1.1.1) from Saccharomyces cerevisiae has been shown to be the site where the substrate activation cascade is triggered [Baburina et al. (1994) Biochem...

2,2'-[(E)-3-(4-Nitro-phen-yl)prop-2-ene-1,1-di-yl]bis-(3-hy-droxy-5,5-dimethyl-cyclo-hex-2-en-1-one).

Acta Crystallogr. Sect. E Struct. Rep. Online 68(8) , o2510-o2510, (2012)

In the title compound, C(25)H(29)NO(6), each of the cyclo-hexenone rings adopts a half-chair conformation. The hy-droxy and carbonyl O atoms face each other and are oriented to allow for the formation...

Genotoxicity of p-nitrocinnamaldehyde and related alpha, beta-unsaturated carbonyl compounds in two bacterial assays.

Mutagenesis 6(4) , 261-9, (1991)

Seventeen cinnamaldehydes, cinnamic acids, 2-furylacroleins and related compounds were tested in the Salmonella preincubation reversion assay and in the SOS chromotest. Of eight compounds containing n...


More Articles


Related Compounds

  • Ethyl 3-(1-methylpyrrolidin-2-yl)prop-2-ynoate
  • 1-[3-Amino-4-(2-methylpropyl)piperidin-1-yl]-3-methylbut-2-en-1-one
  • 6-(4-acetylphenyl)-3-hydroxy-1H,2H,3H,5H-imidazolidino[1,2-a]pyrimidin-5-one
  • 2-(2-Chloro-5-phenylmethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,1,1-Trifluoro-3-(pyrimidin-5-yl)propan-2-ol
  • (3-Ethoxy-2-fluorophenyl)(methyl)sulfane
  • rel-(-)-6,6a(2)-Bis[(S)-methylsulfinyl]-2,2a(2)-bipyridine
  • 4-(1-{[2-(Trifluoromethyl)phenyl]methyl}piperidine-4-carbonyl)thiomorpholine
  • 5-Chloro-2-[3-(4,4-difluoropiperidine-1-carbonyl)pyrrolidin-1-yl]-1,3-benzoxazole
  • 2-Methyl-3-[3-(thiomorpholine-4-carbonyl)pyrrolidin-1-yl]quinoxaline
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