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8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:933190-51-3
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G
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Products Intro: Product Name:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE
CAS:933190-51-3
Purity:98% Package:5KG;1KG
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Products Intro: Product Name:8-Bromo-6-chloroimidazo[1,2-b]pyridazine
CAS:933190-51-3
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Products Intro: Product Name:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE
CAS:933190-51-3
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE
CAS:933190-51-3

8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE manufacturers

8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE Basic information
Application
Product Name:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE
Synonyms:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE;IMidazo[1,2-b]pyridazine, 8-broMo-6-chloro-;8-broMo-6-chloroiMidazo[1;8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE ISO 9001:2015 REACH
CAS:933190-51-3
MF:C6H3BrClN3
MW:232.47
EINECS:
Product Categories:
Mol File:933190-51-3.mol
8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE Structure
8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE Chemical Properties
density 2.03±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka0.73±0.30(Predicted)
AppearanceLight yellow to brown Solid
InChIInChI=1S/C6H3BrClN3/c7-4-3-5(8)10-11-2-1-9-6(4)11/h1-3H
InChIKeyLZEJQXOCRMRVNP-UHFFFAOYSA-N
SMILESC12=NC=CN1N=C(Cl)C=C2Br
Safety Information
MSDS Information
8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE Usage And Synthesis
Application8-Bromo-6-chloroimidazole[1,2-B]pyridazine is a pyridazine organic compound that can be used as a pharmaceutical intermediate.
Synthesis
3-Amino-4-bromo-6-chloropyridazine

446273-59-2

Chloroacetaldehyde diethyl acetal

621-62-5

8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE

933190-51-3

3-Amino-4-bromo-6-chloropyridazine (15.7 g, 75.3 mmol) and chloroacetaldehyde diethyl acetal (13.9 g, 90.3 mmol) were reacted in isopropanol (150 mL) in the presence of p-toluenesulfonic acid (PTSA, 17.2 g, 90.3 mmol). The reaction mixture was heated to 80 °C and maintained at this temperature for 20 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure to remove the solvent. The concentrated residue was neutralized with saturated sodium bicarbonate solution (300 mL) and then extracted with dichloromethane (200 mL × 3). The organic layers were combined, dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (200-300 mesh, petroleum ether:ethyl acetate = 3:1) to afford the target product, 8-bromo-6-chloroimidazo[1,2-b]pyridazine (17.2 g, 98% yield), as an orange solid.LC-MS analysis showed [M + H]+ m/z 231.9, 233.9, and retention time tR = 1.46 min.

References[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 23, p. 10414 - 10423
[2] Patent: US2013/109661, 2013, A1. Location in patent: Paragraph 0227-0228
[3] Patent: WO2013/64445, 2013, A1. Location in patent: Page/Page column 51
8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE Preparation Products And Raw materials
Raw materialsChloroacetaldehyde-->3-Amino-4-bromo-6-chloropyridazine-->Chloroacetaldehyde diethyl acetal-->p-Toluenesulfonic acid monohydrate-->Isopropyl alcohol
Tag:8-BROMO-6-CHLOROIMIDAZO[1,2-B]PYRIDAZINE(933190-51-3) Related Product Information
Imidazo[1,2-b]pyridazine 6-Chloroimidazo[2,1-f]pyridazine

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