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
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)
Safety
- HS Code
- 2933998090
N-Bromosuccinimide Price
- Product number
- C994365
- Product name
- 3-Chloro-6-(methylsulfonyl)pyridazine
- Packaging
- 500mg
- Price
- $285
- Updated
- 2021/12/16
- Product number
- FC144116
- Product name
- 3-Chloro-6-(methylsulfonyl)pyridazine
- Packaging
- 50mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- FC144116
- Product name
- 3-Chloro-6-(methylsulfonyl)pyridazine
- Packaging
- 100mg
- Price
- $120
- Updated
- 2021/12/16
- Product number
- FC144116
- Product name
- 3-Chloro-6-(methylsulfonyl)pyridazine
- Packaging
- 250mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- OR903459
- Product name
- 3-Chloro-6-(methylsulfonyl)pyridazine
- Purity
- 95%
- Packaging
- 250mg
- Price
- $218
- Updated
- 2021/12/16
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
3-Chloro-6-(methylsulfonyl)pyridazine Suppliers
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