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2-Fluoro-6-nitrobenzoic acid methyl ester

Product Name
2-Fluoro-6-nitrobenzoic acid methyl ester
CAS No.
212189-78-1
Chemical Name
2-Fluoro-6-nitrobenzoic acid methyl ester
Synonyms
Benzoic acid, 2-fluoro-6-nitro-, methyl ester
CBNumber
CB52745151
Molecular Formula
C8H6FNO4
Formula Weight
199.14
MOL File
212189-78-1.mol
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2-Fluoro-6-nitrobenzoic acid methyl ester Property

Boiling point:
282.9±25.0 °C(Predicted)
Density 
1.388±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety

HS Code 
2916399090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M706748
Product name
Methyl2-fluoro-6-nitrobenzoate
Packaging
1mg
Price
$45
Updated
2021/12/16
TRC
Product number
M706748
Product name
Methyl2-fluoro-6-nitrobenzoate
Packaging
10mg
Price
$75
Updated
2021/12/16
SynQuest Laboratories
Product number
4654-3-8D
Product name
Methyl 2-fluoro-6-nitrobenzoate
Packaging
250mg
Price
$168
Updated
2021/12/16
SynQuest Laboratories
Product number
4654-3-8D
Product name
Methyl 2-fluoro-6-nitrobenzoate
Packaging
1g
Price
$272
Updated
2021/12/16
Matrix Scientific
Product number
083249
Product name
Methyl 2-fluoro-6-nitrobenzoate
Purity
97%
Packaging
1g
Price
$414
Updated
2021/12/16
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2-Fluoro-6-nitrobenzoic acid methyl ester Chemical Properties,Usage,Production

Synthesis

385-02-4

18107-18-1

212189-78-1

General procedure for the synthesis of methyl 2-fluoro-6-nitrobenzoate from 2-fluoro-6-nitrobenzoic acid and trimethylsilylated diazomethane: 2-fluoro-6-nitrobenzoic acid (712 mg, 3.85 mmol) was dissolved in a mixed solvent of methanol/acetonitrile (10 mL/10 mL) under nitrogen protection and cooled to 0 °C. Trimethylsilylated diazomethane solution was slowly added dropwise until the reaction solution took on a persistent yellow color, and stirring was continued at 0 °C for 30 min. Subsequently, the reaction was quenched with glacial acetic acid until the yellow color disappeared. The solvent was partially evaporated under reduced pressure and the residue was dissolved in a small amount of ethyl acetate and purified by fast column chromatography using 30%-50% ethyl acetate/hexane (600 mL) as eluent to afford the target product methyl 2-fluoro-6-nitrobenzoate (716 mg, 94% yield). The product characterization data were as follows: 1H NMR (400 MHz, CDCl3) δ 3.96 (s, 3H), 7.40-7.48 (m, 1H), 7.58 (td, J = 8.31,5.54 Hz, 1H), 7.94 (d, J = 8.31 Hz, 1H); mass spectrometry (MS) m/z 200.05 (MH+), calculated value ( C8H6FNO4) 199.03.

References

[1] Patent: US2006/94707, 2006, A1. Location in patent: Page/Page column 66
[2] Patent: US2007/259850, 2007, A1. Location in patent: Page/Page column 100
[3] Patent: WO2008/51547, 2008, A1. Location in patent: Page/Page column 406

2-Fluoro-6-nitrobenzoic acid methyl ester Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Fluoro-6-nitrobenzoic acid methyl ester Suppliers

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