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3-bromo-6-methylpyridazine

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Products Intro: Product Name:3-bromo-6-methylpyridazine 6-Methyl-3-broMopyridazine
CAS:65202-58-6
Purity:98%minHPLC Package:1KG|5KG
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Products Intro: Product Name:3-Bromo-6-methylpyridazine
CAS:65202-58-6
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Products Intro: Product Name:3-Bromo-6-Methylpyridazine
CAS:65202-58-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:3-bromo-6-methylpyridazine
CAS:65202-58-6
Purity:98% HPLC Package:5G,10G,25G,50G,100G,250G,1KG
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Products Intro: Product Name:3-Bromo-6-methylpyridazine
CAS:65202-58-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-15907

3-bromo-6-methylpyridazine manufacturers

3-bromo-6-methylpyridazine Basic information
Product Name:3-bromo-6-methylpyridazine
Synonyms:3-bromo-6-methylpyridazine;Pyridazine, 3-broMo-6-Methyl-;6-Methyl-3-broMopyridazine;3-bromo-6-methylpyridazine 6-Methyl-3-broMopyridazine;3-bromo-6-methylpyridazine ISO 9001:2015 REACH
CAS:65202-58-6
MF:C5H5BrN2
MW:173.01
EINECS:
Product Categories:
Mol File:65202-58-6.mol
3-bromo-6-methylpyridazine Structure
3-bromo-6-methylpyridazine Chemical Properties
Boiling point 285.0±20.0 °C(Predicted)
density 1.596±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
pka1.26±0.10(Predicted)
form Solid
color Dark Brown
InChIInChI=1S/C5H5BrN2/c1-4-2-3-5(6)8-7-4/h2-3H,1H3
InChIKeyRACIHBXDZONTQJ-UHFFFAOYSA-N
SMILESC1(Br)=NN=C(C)C=C1
Safety Information
HS Code 2933998090
MSDS Information
3-bromo-6-methylpyridazine Usage And Synthesis
Uses3-Bromo-6-methylpyridazine is used as a reagent in the synthesis of piperazinyl quinolines as chemosensitizers to increase fluconazole susceptibility of Candida albicans. 3-Bromo-6-methylpyridazine is also used in the preparation of cyclohexyl fluoropyrimidinyl benzamides as CNS penetrable P2X7 receptor antagonists.
Synthesis
6-Methylpyridazin-3(2H)-one

13327-27-0

3-bromo-6-methylpyridazine

65202-58-6

6-Methyl-3(2H)-pyridazinone (18 g, 163.44 mmol) was mixed with phosphorus tribromide oxide (93.8 g, 327.6 mmol) and the reaction was stirred at 70 °C overnight. Upon completion of the reaction, the reaction mixture was cooled to 40 °C and quenched by slowly pouring it into ice water. Subsequently, the reaction mixture was neutralized with saturated sodium bicarbonate solution (20 mL) and extracted with dichloromethane (100 mL x 3). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product 3-bromo-6-methylpyridazine (8 g, 31% yield). The product was detected by LCMS (ESI), m/z: 173 [M + 1]+. 1H NMR (chloroform-d, Bruker Avance 400MHz) data were as follows: δ 7.86-7.88 (d, 1H, J = 8Hz), 7.52-7.54 (d, 1H, J = 8Hz), 2.55 (s, 3H).

References[1] Patent: EP3333157, 2018, A1. Location in patent: Paragraph 0136; 0137
[2] Patent: WO2010/36998, 2010, A2. Location in patent: Page/Page column 184
3-bromo-6-methylpyridazine Preparation Products And Raw materials
Raw materialsMethanesulfonic acid, 1,1,1-trifluoro-, 6-methyl-3-pyridazinyl ester-->6-Methylpyridazin-3(2H)-one
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