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Methyl 6-broMo-2-Methoxynicotinate

Product Name
Methyl 6-broMo-2-Methoxynicotinate
CAS No.
1009735-24-3
Chemical Name
Methyl 6-broMo-2-Methoxynicotinate
Synonyms
Methyl 6-broMo-2-Methoxynicotinate;6-bromo-2-methoxynicotinic acid methyl ester;methyl 6-bromo-2-methoxy-pyridine-3-carboxylate;3-Pyridinecarboxylic acid, 6-bromo-2-methoxy-, methyl ester
CBNumber
CB42732963
Molecular Formula
C8H8BrNO3
Formula Weight
246.06
MOL File
1009735-24-3.mol
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Methyl 6-broMo-2-Methoxynicotinate Property

Boiling point:
296.5±35.0 °C(Predicted)
Density 
1.530±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-3.08±0.10(Predicted)
Appearance
White to light yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
2759DV
Product name
Methyl6-bromo-2-methoxynicotinate
Packaging
250mg
Price
$288
Updated
2021/12/16
AK Scientific
Product number
2759DV
Product name
Methyl6-bromo-2-methoxynicotinate
Packaging
5g
Price
$1724
Updated
2021/12/16
AK Scientific
Product number
2759DV
Product name
Methyl6-bromo-2-methoxynicotinate
Packaging
10g
Price
$2548
Updated
2021/12/16
Alichem
Product number
1009735243
Product name
Methyl6-bromo-2-methoxynicotinate
Packaging
5g
Price
$1824.47
Updated
2021/12/16
Ambeed
Product number
A378813
Product name
Methyl6-bromo-2-methoxynicotinate
Purity
98%
Packaging
10g
Price
$1843
Updated
2021/12/16
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Methyl 6-broMo-2-Methoxynicotinate Chemical Properties,Usage,Production

Synthesis

1060806-62-3

74-88-4

1009735-24-3

Step 2: Synthesis of methyl 6-bromo-2-methoxynicotinate; To N,N-dimethylformamide (10 mL), potassium carbonate (1.34 g, 9.48 mmol), 6-bromo-2-methoxynicotinic acid (1.10 g, 4.74 mmol), and iodomethane (0.895 g, 6.31 mmol) were added sequentially. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the reaction mixture was diluted with water and ethyl acetate and the organic and aqueous layers were separated. The aqueous layer was extracted twice with ethyl acetate. All organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography using 5%-10% ethyl acetate/heptane gradient elution to afford methyl 6-bromo-2-methoxynicotinate as a colorless oil (0.459 g, 40% yield).1H NMR (500 MHz, DMSO-d6) δppm3.81 (3H, s), 3.93 (3H, s), 7.36 (1H, d, J = 7.8 Hz), 8.06 (1H, d, J = 7.8 Hz).

References

[1] Patent: WO2010/116282, 2010, A1. Location in patent: Page/Page column 60
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 10, p. 4273 - 4288

Methyl 6-broMo-2-Methoxynicotinate Preparation Products And Raw materials

Raw materials

Preparation Products

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Methyl 6-broMo-2-Methoxynicotinate Suppliers

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