Basic information Safety Supplier Related

2-FLUORO-5-NITROBENZYL ALCOHOL 96

Basic information Safety Supplier Related

2-FLUORO-5-NITROBENZYL ALCOHOL 96 Basic information

Product Name:
2-FLUORO-5-NITROBENZYL ALCOHOL 96
Synonyms:
  • 2-FLUORO-5-NITROBENZYL ALCOHOL 96
  • (2-Fluoro-5-nitrophenyl)methanol
  • 2-Fluoro-5-nitrophenyl alcohol
  • 2-Fluoro-5-nitronbenzyl alcohol
  • 2-Fluoro-5-nitrobenzyl alcohol 96%
  • 2-Fluoro-5-nitrobenzenemethanol
  • 2-Fluoro-5-nitrobenzyl alcohol 95+%
  • Benzenemethanol, 2-fluoro-5-nitro-
CAS:
63878-73-9
MF:
C7H6FNO3
MW:
171.13
Product Categories:
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
  • Aryl Fluorinated Building Blocks
  • Building Blocks
  • C7
  • C7 to C8
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Oxygen Compounds
Mol File:
63878-73-9.mol
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2-FLUORO-5-NITROBENZYL ALCOHOL 96 Chemical Properties

Melting point:
68-71 °C (lit.)
Boiling point:
319.0±27.0 °C(Predicted)
Density 
1.434±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
13.34±0.10(Predicted)
Appearance
Yellow to brown Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2906290090
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2-FLUORO-5-NITROBENZYL ALCOHOL 96 Usage And Synthesis

Uses

2-Fluoro-5-nitrobenzyl alcohol may be used to synthesize 2-fluoro-5-nitrobenzyl bromide and 5-amino-2-fluorobenzyl alcohol.

General Description

2-Fluoro-5-nitrobenzyl alcohol can be prepared from 2-fluoro-5-nitrobenzaldehyde.

Synthesis

27996-87-8

63878-73-9

General steps for the synthesis of 2-fluoro-5-nitrobenzyl alcohol from 2-fluoro-5-nitrobenzaldehyde: Step A: Preparation of (2-fluoro-5-nitrobenzyl)methanol To a solution of 2-fluoro-5-nitrobenzaldehyde (1000 mg, 5.91 mmol) in methanol (10 mL) was added sodium borohydride (182 mg, 4.82 mmol). The reaction mixture was stirred at 0 °C for 3 hours. Upon completion of the reaction, the reaction mixture was acidified to pH 4 with 1 M hydrochloric acid and then concentrated. 50 mL of water was added and the product was extracted with ether. The organic layer was dried with magnesium sulfate, filtered and the solvent was evaporated. The target compound (2-fluoro-5-nitrophenyl)methanol was obtained as a light yellow solid (1007 mg, 99% yield) with a melting point of 62-64 °C. 1H NMR (300 MHz, CDCl3) δ 8.43 (dd, 6-CH, J = 6.2 Hz and 2.9 Hz, 1H), 8.19 (ddd, J = 9 Hz, 4.5 Hz and 2.9 Hz, 1H), 7.20 (dd, J = 9.0 Hz and 9.0 Hz, 1H), 4.85 (d, J = 3.6 Hz, 2H), 2.12 (s, 1H). 13C NMR (75 MHz, CDCl3) δ 125.0 (CH, d, J = 10.0 Hz), 124.7 (CH, d, J = 6.9 Hz), 116.2 (CH, d, J = 23.6 Hz), 58.2 (CH2).

References

[1] Heterocyclic Communications, 2010, vol. 16, # 4-6, p. 235 - 239
[2] Patent: WO2011/73322, 2011, A1. Location in patent: Page/Page column 48
[3] Patent: US2017/369489, 2017, A1. Location in patent: Paragraph 0453; 0465
[4] Journal of Heterocyclic Chemistry, 2008, vol. 45, # 2, p. 547 - 550
[5] Chemistry - A European Journal, 2015, vol. 21, # 32, p. 11462 - 11474

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