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2-Fluoro-3-nitrobenzoic acid

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Company Name: Fluoropharm Co., Ltd.
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Products Intro: Product Name:2-Fluoro-3-nitrobenzoic acid
CAS:317-46-4
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Products Intro: Product Name:2-Fluoro-3-nitrobenzoic acid
CAS:317-46-4
Purity:0.98
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Products Intro: Product Name:2-FLUORO-3-NITROBENZOIC ACID
CAS:317-46-4
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CAS:317-46-4
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Products Intro: Product Name:2-Fluoro-3-nitrobenzoic acid
CAS:317-46-4
Purity:99.00% Package:1g;1.1USD

2-Fluoro-3-nitrobenzoic acid manufacturers

2-Fluoro-3-nitrobenzoic acid Basic information
Product Name:2-Fluoro-3-nitrobenzoic acid
Synonyms:Benzoic acid,2-fluoro-3-nitro-;2-FLUORO-3-NITROBENZOIC ACID;2-Fluoro-3-nitrobenzoic acid+B244;2-Fluoro-3-nitrobenzoic acid 99%;3-Carboxy-2-fluoronitrobenzene;3-Pyridinecarboxylic acid, 4-aMino-
CAS:317-46-4
MF:C7H4FNO4
MW:185.11
EINECS:630-017-4
Product Categories:Fluorine series;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:317-46-4.mol
2-Fluoro-3-nitrobenzoic acid Structure
2-Fluoro-3-nitrobenzoic acid Chemical Properties
Melting point 138 - 140°C
Boiling point 347.6±27.0 °C(Predicted)
density 1.568±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO (Sparingly), Methanol (Slightly)
pka2.32±0.20(Predicted)
form Solid
color White to Off-White
Water Solubility Slightly soluble in water.
Sensitive Air Sensitive
Stability:Hygroscopic
InChIInChI=1S/C7H4FNO4/c8-6-4(7(10)11)2-1-3-5(6)9(12)13/h1-3H,(H,10,11)
InChIKeyWLGUSLGYTNJJFV-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC=CC([N+]([O-])=O)=C1F
Safety Information
Hazard Codes Xi
Safety Statements 24/25
HS Code 29163990
MSDS Information
2-Fluoro-3-nitrobenzoic acid Usage And Synthesis
Chemical PropertiesLight yellow crystalline powder
Uses2-Fluoro-3-nitrobenzoic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
SynthesisConcentrated sulfuric acid (195 ml) was added carefully and stirred to a solution of 2-fluoro-3-nitrotoluene (100 g, 645 mmol) in acetic acid (1000 ml). The mixture was warmed up to 95° C. The chromium trioxide solution (226 g, 2.25 mol) in water (200 ml) was added dropwise while stirring for over 2 h. After addition, the mixture was heated by stirring for another 3 h, allowed to cool down to room temperature, and poured into water (3 L). The mixture was extracted with ethyl acetate (3.x.1 L), the combined organic layers were dried over Na2SO4and concentrated under reduced pressure to afford a light green solid, which was washed with dichloromethane (3.x.300 ml) and dried under vacuum to afford 2-Fluoro-3-nitrobenzoic acid was obtained as a light yellow solid (75 g, 62.8percent). 1H NMR (300 MHz, DMSO) δ ppm 8.27 (m, 1H), 8.15 (m, 1H), 7.48 (m, 1H).
References[1] Patent: US2009/298815, 2009, A1. Location in patent: Page/Page column 53
[2] Patent: WO2011/59610, 2011, A1. Location in patent: Page/Page column 87-88
Tag:2-Fluoro-3-nitrobenzoic acid(317-46-4) Related Product Information
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