Basic information Safety Supplier Related

4-HYDROXY-B-NITROSTYRENE

Basic information Safety Supplier Related

4-HYDROXY-B-NITROSTYRENE Basic information

Product Name:
4-HYDROXY-B-NITROSTYRENE
Synonyms:
  • 1-(4-HYDROXYPHENYL)-2-NITROETHENE
  • 4-Hydroxy--nitrostyrene
  • 4-(2-Nitrovinyl)phenol
  • 2-(4-HYDROXYPHENYL)NITROETHENE
  • 1-HYDROXY-4-(2-NITROVINYL)BENZENE
  • 4'-HYDROXY-BETA-NITROSTYRENE
  • 4-HYDROXY-BETA-NITROSTYRENE
  • 4-HYDROXY-B-NITROSTYRENE
CAS:
3179-08-6
MF:
C8H7NO3
MW:
165.15
Mol File:
3179-08-6.mol
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4-HYDROXY-B-NITROSTYRENE Chemical Properties

Melting point:
167-171 °C(lit.)
Boiling point:
318.3±17.0 °C(Predicted)
Density 
1.320±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.04±0.13(Predicted)
Appearance
Yellow to brown Solid
InChI
InChI=1S/C8H7NO3/c10-8-3-1-7(2-4-8)5-6-9(11)12/h1-6,10H
InChIKey
CTJKRKMPTRJAIT-UHFFFAOYSA-N
SMILES
C1(O)=CC=C(C=C[N+]([O-])=O)C=C1
CAS DataBase Reference
3179-08-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2908990000

MSDS

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4-HYDROXY-B-NITROSTYRENE Usage And Synthesis

Synthesis

7400-08-0

3179-08-6

General procedure for the synthesis of 4-(2-nitrovinyl)phenol from 4-hydroxycinnamic acid: 0.01 mol of 4-hydroxycinnamic acid, about 0.01 mol of TCICA/DMF reagent, 1 g of sodium nitrite, and 25 mL of CH2Cl2 or acetonitrile were added to a pre-cleaned round-bottomed flask with stirring and the reaction was carried out under refluxing conditions for 8 to 10 hours. The progress of the reaction was monitored by TLC. Upon completion of the reaction, the reaction mixture was washed with NaHCO3 solution and subsequently extracted with ethyl acetate. The organic layer was separated, dried with anhydrous MgSO4 and concentrated in vacuum. Finally, purification by column chromatography using ethyl acetate-hexane as eluent gave the pure product 4-(2-nitrovinyl)phenol as a yellow powder.

References

[1] Synthetic Communications, 2013, vol. 43, # 19, p. 2672 - 2677
[2] Catalysis Science and Technology, 2016, vol. 6, # 5, p. 1430 - 1434
[3] Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry, 2013, vol. 43, # 8, p. 977 - 983
[4] Synthetic Communications, 2015, vol. 45, # 19, p. 2251 - 2258

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