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2,6-dibroMo-3-Methoxy-5-nitropyridine

Product Name
2,6-dibroMo-3-Methoxy-5-nitropyridine
CAS No.
79491-46-6
Chemical Name
2,6-dibroMo-3-Methoxy-5-nitropyridine
Synonyms
2,6-dibroMo-3-Methoxy-5-nitropyridine;Pyridine, 2,6-dibromo-3-methoxy-5-nitro-
CBNumber
CB52605983
Molecular Formula
C6H4Br2N2O3
Formula Weight
311.92
MOL File
79491-46-6.mol
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2,6-dibroMo-3-Methoxy-5-nitropyridine Property

Melting point:
113-114 °C(Solv: ligroine (8032-32-4))
Boiling point:
342.5±37.0 °C(Predicted)
Density 
2.067±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-12.06±0.10(Predicted)
Appearance
Light yellow to orange Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HCH0362896
Product name
2,6-DIBROMO-3-METHOXY-5-NITROPYRIDINE
Purity
95.00%
Packaging
5MG
Price
$498.36
Updated
2021/12/16
AK Scientific
Product number
5635BB
Product name
2,6-Dibromo-3-methoxy-5-nitropyridine
Packaging
10g
Price
$1154
Updated
2021/12/16
Crysdot
Product number
CD11055606
Product name
2,6-Dibromo-3-methoxy-5-nitropyridine
Purity
97%
Packaging
10g
Price
$1169
Updated
2021/12/16
Alichem
Product number
79491466
Product name
2,6-Dibromo-3-methoxy-5-nitropyridine
Packaging
10g
Price
$1180
Updated
2021/12/16
Acints
Product number
ACI-03881
Product name
2,6-Dibromo-3-methoxy-5-nitro-pyridine
Purity
95%+
Packaging
5g
Price
$1442.75
Updated
2021/12/16
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2,6-dibroMo-3-Methoxy-5-nitropyridine Chemical Properties,Usage,Production

Synthesis

79491-45-5

79491-46-6

The general procedure for the synthesis of 2,6-dibromo-3-methoxy-5-nitropyridine using 2,6-dibromo-3-methoxypyridine as starting material was as follows: first, concentrated sulfuric acid (16 mL) was slowly added to the reaction vessel at 0 °C. Subsequently, 2,6-dibromo-3-methoxypyridine (3.4 g, 13 mmol) was added in batches, and the process was completed within 20 min. Next, 90% fuming nitric acid (16 mL, 318 mmol) was added dropwise to the reaction system. After installing a reflux condenser, the reaction mixture was gradually warmed to room temperature, then heated to 65 °C and maintained at this temperature for 2 hours. Upon completion of the reaction, the mixture was slowly poured into a 500 mL beaker containing ice. After the ice was completely melted, the mixture was vacuum filtered and the resulting solid was washed with a small amount of cold water. Finally, the collected solid was dried under vacuum to afford the target product 2,6-dibromo-3-methoxy-5-nitropyridine (1.67 g, 5.4 mmol) in 42% yield as a light yellow solid.

References

[1] Australian Journal of Chemistry, 1981, vol. 34, # 4, p. 927 - 932
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 24, p. 5630 - 5634
[3] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 15, p. 4298 - 4311
[4] Patent: EP2017277, 2009, A1. Location in patent: Page/Page column 30

2,6-dibroMo-3-Methoxy-5-nitropyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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2,6-dibroMo-3-Methoxy-5-nitropyridine Suppliers

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79491-46-6, 2,6-dibroMo-3-Methoxy-5-nitropyridineRelated Search:


  • 2,6-dibroMo-3-Methoxy-5-nitropyridine
  • Pyridine, 2,6-dibromo-3-methoxy-5-nitro-
  • 79491-46-6