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3-Chloro-6-(methylsulfonyl)pyridazine

Product Name
3-Chloro-6-(methylsulfonyl)pyridazine
CAS No.
7145-62-2
Chemical Name
3-Chloro-6-(methylsulfonyl)pyridazine
Synonyms
NSC 74444;3-Chloro-6-(methylsulfonyl);3-bromo-6-(methylsulfonyl)pyridazine;3-Chloro-6-(methylsulfonyl)pyridazine;Pyridazine, 3-chloro-6-(methylsulfonyl)-
CBNumber
CB62499013
Molecular Formula
C5H5ClN2O2S
Formula Weight
192.62
MOL File
7145-62-2.mol
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3-Chloro-6-(methylsulfonyl)pyridazine Property

Boiling point:
451.4±45.0 °C(Predicted)
Density 
1.486±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.66±0.10(Predicted)
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Safety

HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C994365
Product name
3-Chloro-6-(methylsulfonyl)pyridazine
Packaging
500mg
Price
$285
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC144116
Product name
3-Chloro-6-(methylsulfonyl)pyridazine
Packaging
50mg
Price
$75
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC144116
Product name
3-Chloro-6-(methylsulfonyl)pyridazine
Packaging
100mg
Price
$120
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC144116
Product name
3-Chloro-6-(methylsulfonyl)pyridazine
Packaging
250mg
Price
$200
Updated
2021/12/16
Apolloscientific
Product number
OR903459
Product name
3-Chloro-6-(methylsulfonyl)pyridazine
Purity
95%
Packaging
250mg
Price
$218
Updated
2021/12/16
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3-Chloro-6-(methylsulfonyl)pyridazine Chemical Properties,Usage,Production

Synthesis

7145-61-1

7145-62-2

The general procedure for the synthesis of 3-chloro-6-(methylthio)pyridazine from 3-chloro-6-(methylsulfonyl)pyrazine was as follows: 3-chloro-6-(methylthio)pyridazine (90 mg, 0.50 mmol) was dissolved in dichloromethane (10 mL), and isochloroperbenzoic acid (220 mg, 1.00 mmol) was added. The reaction mixture was stirred at 0 °C for 30 min under nitrogen protection. After completion of the reaction, water (20 mL) was added to the reaction solution and extracted twice with dichloromethane (10 mL). The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, gradient elution, 10%-100%) to afford the target compound 3-chloro-6-(methylsulfonyl)pyrazine (77 mg, 71% yield) as a white solid.1H-NMR (CDCl3, 400 MHz) data were as follows:δ 3.45 (3H, s) 7.81 (1H, d, J = 8.2Hz), 8.16 (1H, d, J = 8.4Hz).

References

[1] Patent: EP2239253, 2010, A1. Location in patent: Page/Page column 156
[2] Yakugaku Zasshi, 1955, vol. 75, p. 1242,1243
[3] Yakugaku Zasshi, 1956, vol. 76, p. 765
[4] Chem.Abstr., 1957, p. 1192
[5] Patent: WO2015/17305, 2015, A1. Location in patent: Page/Page column 65

3-Chloro-6-(methylsulfonyl)pyridazine Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Chloro-6-(methylsulfonyl)pyridazine Suppliers

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7145-62-2, 3-Chloro-6-(methylsulfonyl)pyridazineRelated Search:


  • 3-Chloro-6-(methylsulfonyl)pyridazine
  • 3-bromo-6-(methylsulfonyl)pyridazine
  • NSC 74444
  • 3-Chloro-6-(methylsulfonyl)
  • Pyridazine, 3-chloro-6-(methylsulfonyl)-
  • 7145-62-2