ChemicalBook > CAS DataBase List > 3,6-Dibromo-2,4-dimethylpyridine

3,6-Dibromo-2,4-dimethylpyridine

Product Name
3,6-Dibromo-2,4-dimethylpyridine
CAS No.
5006-57-5
Chemical Name
3,6-Dibromo-2,4-dimethylpyridine
Synonyms
3,6-Dibromo-2,4-dimethylpyridine;Pyridine, 3,6-dibromo-2,4-dimethyl-
CBNumber
CB03064485
Molecular Formula
C7H7Br2N
Formula Weight
264.95
MOL File
5006-57-5.mol
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3,6-Dibromo-2,4-dimethylpyridine Property

Boiling point:
270.1±35.0 °C(Predicted)
Density 
1.795±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-0.20±0.18(Predicted)
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

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

Ambeed
Product number
A255928
Product name
3,6-Dibromo-2,4-dimethylpyridine
Purity
95%
Packaging
100mg
Price
$56
Updated
2021/12/16
Ambeed
Product number
A255928
Product name
3,6-Dibromo-2,4-dimethylpyridine
Purity
95%
Packaging
250mg
Price
$111
Updated
2021/12/16
Ambeed
Product number
A255928
Product name
3,6-Dibromo-2,4-dimethylpyridine
Purity
95%
Packaging
1g
Price
$277
Updated
2021/12/16
Chemenu
Product number
CM125433
Product name
3,6-dibromo-2,4-dimethylpyridine
Purity
95%
Packaging
1g
Price
$308
Updated
2021/12/16
Crysdot
Product number
CD11115620
Product name
3,6-Dibromo-2,4-dimethylpyridine
Purity
95+%
Packaging
1g
Price
$510
Updated
2021/12/16
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3,6-Dibromo-2,4-dimethylpyridine Chemical Properties,Usage,Production

Synthesis

89856-44-0

5006-57-5

The general procedure for the synthesis of 3,6-dibromo-2,4-dimethylpyridine starting from 2-amino-5-bromo-4,6-dimethylpyridine was as follows: 2-amino-5-bromo-4,6-dimethylpyridine (201 mg, 1 mmol) was dissolved in 48% hydrobromic acid (3 mL) at 0 °C, and slowly added dropwise to sodium nitrite (172 mg, 2.5 mmol) in an aqueous solution (0.6 mL). The reaction mixture was stirred at 0-5 °C for 30 min, then bromine (448 mg, 2.8 mmol) was added and the reaction temperature was ensured not to exceed 5 °C. The reaction mixture was stirred at 0-5 °C for 30 min. After continued stirring for 30 min, the reaction mixture was adjusted to alkaline with 20% cold sodium hydroxide solution. Subsequently, it was extracted three times with ethyl acetate, the organic layers were combined and dried with anhydrous sodium sulfate, filtered and concentrated. Finally, the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate, 10:1) to afford the light yellow solid product 3,6-dibromo-2,4-dimethylpyridine (243 mg, 92% yield).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 5093 - 5097
[2] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 395 - 408,14
[3] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 395 - 408

3,6-Dibromo-2,4-dimethylpyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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3,6-Dibromo-2,4-dimethylpyridine Suppliers

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5006-57-5, 3,6-Dibromo-2,4-dimethylpyridineRelated Search:


  • 3,6-Dibromo-2,4-dimethylpyridine
  • Pyridine, 3,6-dibromo-2,4-dimethyl-
  • 5006-57-5