Basic information Safety Supplier Related

5-HYDROXY-2-NITROBENZYL ALCOHOL

Basic information Safety Supplier Related

5-HYDROXY-2-NITROBENZYL ALCOHOL Basic information

Product Name:
5-HYDROXY-2-NITROBENZYL ALCOHOL
Synonyms:
  • 5-HYDROXY-2-NITROBENZYL ALCOHOL
  • RARECHEM AL BD 0679
  • 2-Nitro-5-hydroxybenzenemethanol
  • 2-Nitro-5-hydroxybenzyl alcohol
  • 3-(Hydroxymethyl)-4-nitrophenol
  • 5-Hydroxy-2-nitrobenzenemethanol
  • (5-Hydroxy-2-nitrophenyl)methanol
  • 5-Hydroxy-2-nitrobenzyl alcohol 97%
CAS:
60463-12-9
MF:
C7H7NO4
MW:
169.13
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
  • Building Blocks
  • C7 to C8
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
60463-12-9.mol
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5-HYDROXY-2-NITROBENZYL ALCOHOL Chemical Properties

Melting point:
111-115 °C (lit.)
Boiling point:
398.6±32.0 °C(Predicted)
Density 
1.489±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
6.99±0.10(Predicted)
Appearance
Light brown to gray Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3

MSDS

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5-HYDROXY-2-NITROBENZYL ALCOHOL Usage And Synthesis

Uses

5-Hydroxy-2-nitrobenzyl alcohol may be used in the synthesis of 5-(2′-(dimethylamino)ethoxy)-2-nitrobenzyl alcohol. It may be used as difunctional photo-responsive initiator in the synthesis of thermo-responsive and photo-cleavable amphiphilic block copolymers containing photodegradable linkers as junction points between hydrophilic and hydrophobic chains.

Synthesis

42454-06-8

60463-12-9

General procedure for the synthesis of 5-hydroxy-2-nitrobenzaldehyde from 5-hydroxy-2-nitrobenzenemethanol: Sodium borohydride (1.4 g, 37.84 mmol) was slowly added to a solution of 5-hydroxy-2-nitrobenzaldehyde (4.07 g, 24.35 mmol) in methanol (30 mL) while the reaction mixture was cooled in an ice water bath. After the addition was completed, the reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the residue was recrystallized in methanol to give 4.0 g (23.62 mmol, 97% yield) of 5-hydroxy-2-nitrobenzyl alcohol.

References

[1] Angewandte Chemie - International Edition, 2006, vol. 45, # 17, p. 2753 - 2757
[2] Patent: US2007/213278, 2007, A1. Location in patent: Page/Page column 29; Sheet 9
[3] Journal of Polymer Science, Part A: Polymer Chemistry, 2013, vol. 51, # 20, p. 4309 - 4316
[4] Journal of Organic Chemistry, 1998, vol. 63, # 8, p. 2434 - 2441
[5] Chemistry - A European Journal, 2015, vol. 21, # 5, p. 1873 - 1877

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