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METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE

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METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE Basic information

Product Name:
METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE
Synonyms:
  • METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE
  • METHYL 3-FLUORO-4-NITROBENZOATE
  • Methyl 3-fluoro-4-nitrobenzoate 98%
  • Methyl3-fluoro-4-nitrobenzoate98%
  • 3-Fluoro-4-nitrobenzoic acid methyl ester
  • METHYL 3-FLUORO-4-NITROBENZENECARBOXYLAT
  • 2-Fluoro-4-(methoxycarbonyl)nitrobenzene
  • Benzoic acid, 3-fluoro-4-nitro-, methyl ester
CAS:
185629-31-6
MF:
C8H6FNO4
MW:
199.14
Product Categories:
  • blocks
  • Carboxes
Mol File:
185629-31-6.mol
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METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE Chemical Properties

Melting point:
59-61°
Boiling point:
314.6±32.0 °C(Predicted)
Density 
1.388±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
Solid
Appearance
White to off-white Solid
InChI
InChI=1S/C8H6FNO4/c1-14-8(11)5-2-3-7(10(12)13)6(9)4-5/h2-4H,1H3
InChIKey
FKMZNQQOPCCUTD-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C([N+]([O-])=O)C(F)=C1
CAS DataBase Reference
185629-31-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
HazardClass 
IRRITANT
HS Code 
2916399090
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METHYL 3-FLUORO-4-NITROBENZENECARBOXYLATE Usage And Synthesis

Chemical Properties

Light yellow powder

Uses

In chemical research, Methyl 3-fluoro-4-nitrobenzenecarboxylate can be used to explore its chemical properties and reactivity, especially in the study of fluorides and nitro compounds.

Synthesis

67-56-1

403-21-4

185629-31-6

General procedure for the synthesis of methyl 3-fluoro-4-nitrobenzoate from methanol and 3-fluoro-4-nitrobenzoic acid: 3-fluoro-4-nitrobenzoic acid (5.00 g, 27.0 mmol), methanol (40 mL), and an ether solution of 2N HCl were mixed and heated and refluxed for 16 hours. After completion of the reaction, the volatiles were evaporated under reduced pressure. The residue was diluted with ethyl acetate (150 mL), washed sequentially with saturated sodium bicarbonate solution and brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound methyl 3-fluoro-4-nitrobenzoate (5.18 g, 96% yield) as a light yellow solid.

References

[1] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 5, p. 2017 - 2029
[2] Patent: WO2005/80388, 2005, A1. Location in patent: Page/Page column 88-89
[3] Patent: WO2007/16392, 2007, A2. Location in patent: Page/Page column 47
[4] European Journal of Medicinal Chemistry, 2018, vol. 150, p. 156 - 175
[5] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 4, p. 1043 - 1046

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