Basic information Safety Supplier Related

(2-fluoro-4-nitrophenyl)methanol

Basic information Safety Supplier Related

(2-fluoro-4-nitrophenyl)methanol Basic information

Product Name:
(2-fluoro-4-nitrophenyl)methanol
Synonyms:
  • (2-fluoro-4-nitrophenyl)methanol
  • 2-Fluoro-4-nitrobenzyl alcohol, 97%
  • 2-Fluoro-4-nitrobenzyl alcohol 97%
  • 3-Fluoro-4-(hydroxymethyl)nitrobenzene, (2-Fluoro-4-nitrophenyl)methanol
  • 2-Fluoro-4-nitrobenzylalcohol97%
  • Benzenemethanol, 2-fluoro-4-nitro-
CAS:
660432-43-9
MF:
C7H6FNO3
MW:
171.13
Mol File:
660432-43-9.mol
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(2-fluoro-4-nitrophenyl)methanol Chemical Properties

Melting point:
103-105℃
Boiling point:
319.9±27.0 °C(Predicted)
Density 
1.434±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
13.14±0.10(Predicted)
form 
Solid
color 
White to yellow
CAS DataBase Reference
660432-43-9
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Safety Information

HazardClass 
IRRITANT
HS Code 
2906290090
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(2-fluoro-4-nitrophenyl)methanol Usage And Synthesis

Synthesis

157701-72-9

660432-43-9

General procedure for the synthesis of 2-fluoro-4-nitrobenzyl alcohol from 2-fluoro-4-nitrobenzaldehyde: To a solution of 2-fluoro-4-nitrobenzaldehyde (1.0 g, 5.92 mmol) in methanol (10 mL) was slowly added sodium borohydride (814 mg, 22 mmol). The reaction mixture was stirred at room temperature for 15 min and then concentrated by rotary evaporator. The concentrated residue was subjected to liquid-liquid partitioning with ethyl acetate (100 mL) and saturated aqueous sodium chloride solution (100 mL). The combined organic phases were washed with saturated aqueous sodium chloride solution (100 mL x 2) and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated to give the red solid product 2-fluoro-4-nitrobenzyl alcohol (1.0 g, 99% yield).

References

[1] Patent: TWI602818, 2017, B. Location in patent: Paragraph 0481; 0482
[2] Patent: WO2014/173289, 2014, A1. Location in patent: Paragraph 0479; 0481; 0482

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