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Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)

Product Name
Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)
CAS No.
84228-45-5
Chemical Name
Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)
Synonyms
ST5437238;Methyl 4-Amino-2-nitrobenzoate;4-amino-2-nitrobenzoic acid methyl ester;4-amino-2-nitro-benzoic acid methyl ester;Benzoic acid, 4-amino-2-nitro-, methyl ester;Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)
CBNumber
CB71070999
Molecular Formula
C8H8N2O4
Formula Weight
196.16
MOL File
84228-45-5.mol
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Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI) Property

Boiling point:
391.8±22.0 °C(Predicted)
Density 
1.386±0.06 g/cm3(Predicted)
storage temp. 
2-8°C, protect from light
pka
1.22±0.10(Predicted)
Appearance
Yellow to brown Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M224078
Product name
Methyl4-Amino-2-nitrobenzoate
Packaging
500mg
Price
$200
Updated
2021/12/16
Ambeed
Product number
A526900
Product name
Methyl4-amino-2-nitrobenzoate
Purity
98%
Packaging
5g
Price
$280
Updated
2021/12/16
Crysdot
Product number
CD12026264
Product name
Methyl4-amino-2-nitrobenzoate
Purity
95+%
Packaging
25g
Price
$558
Updated
2021/12/16
Ambeed
Product number
A526900
Product name
Methyl4-amino-2-nitrobenzoate
Purity
98%
Packaging
25g
Price
$689
Updated
2021/12/16
Alichem
Product number
84228455
Product name
Methyl4-amino-2-nitrobenzoate
Packaging
500mg
Price
$823.15
Updated
2021/12/16
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Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI) Chemical Properties,Usage,Production

Synthesis

610-36-6

74-88-4

84228-45-5

A suspension was prepared by dissolving 4-amino-2-nitrobenzoic acid (200 mg, 1.10 mmol) and sodium carbonate (349 mg, 3.29 mmol) in dimethylformamide (5.5 mL). Subsequently, iodomethane (0.21 mL) was added to the suspension and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, water was added to the reaction solution and extracted with ethyl acetate. The organic layers were combined and washed sequentially with saturated aqueous ammonium chloride solution and saturated aqueous sodium chloride solution, and then dried over anhydrous sodium sulfate. Concentration of the organic layer by decompression afforded 216 mg of the target product, methyl 4-amino-2-nitrobenzoate, as a yellow solid (100% yield). The product was confirmed by ^1H-NMR (CDCl3, ppm): δ 7.69 (d, J = 8.5 Hz, 1H), 6.85 (d, J = 2.4 Hz, 1H), 6.77 (dd, J = 2.4, 8.5 Hz, 1H), 4.31 (bs, 2H), 3.84 (s, 3H). lC/MS (ESI) showed the molecular ions peaks as 196.

References

[1] Patent: WO2004/108683, 2004, A1. Location in patent: Page 561-562

Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI) Preparation Products And Raw materials

Raw materials

Preparation Products

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Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI) Suppliers

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84228-45-5, Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)Related Search:


  • Methyl 4-Amino-2-nitrobenzoate
  • 4-amino-2-nitrobenzoic acid methyl ester
  • 4-amino-2-nitro-benzoic acid methyl ester
  • ST5437238
  • Benzoic acid, 4-amino-2-nitro-, methyl ester (9CI)
  • Benzoic acid, 4-amino-2-nitro-, methyl ester
  • 84228-45-5
  • AMINOACID