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3-BROMOIMIDAZO[1,2-B]PYRIDAZINE

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Products Intro: Product Name:3-bromoimidazo[1,2-b]pyridazine
CAS:18087-73-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:3-bromoimidazo[1,2-b]pyridazine
CAS:18087-73-5
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Products Intro: CAS:18087-73-5
Purity:98% Package:g-Kg Remarks:Beige crystalline solid
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Products Intro: Product Name:3-BROMOIMIDAZO[1,2-B]PYRIDAZINE
CAS:18087-73-5
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:3-BROMOIMIDAZO[1,2-B]PYRIDAZINE
CAS:18087-73-5
Purity:99% Package:1KG;2USD

3-BROMOIMIDAZO[1,2-B]PYRIDAZINE manufacturers

3-BROMOIMIDAZO[1,2-B]PYRIDAZINE Basic information
Product Name:3-BROMOIMIDAZO[1,2-B]PYRIDAZINE
Synonyms:IMidazo[1,2-b]pyridazine, 3-broMo-;3-BroMoiMidazo[1,2-b]pyri...;3-BROMOIMIDAZO[1,2-B]PYRIDAZINE;3-broMoiMidazo(1,2-b)pyridazin;3-Bromoimidazo[1,2-b]pyridazine;Ponatinib Impurity 2;Ponatinib intermediate;3-Bromoimidazo[1,2-b]pyridazine >
CAS:18087-73-5
MF:C6H4BrN3
MW:198.02
EINECS:
Product Categories:
Mol File:18087-73-5.mol
3-BROMOIMIDAZO[1,2-B]PYRIDAZINE Structure
3-BROMOIMIDAZO[1,2-B]PYRIDAZINE Chemical Properties
Melting point 148.0 to 152.0 °C
density 1.89
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
pka2.35±0.30(Predicted)
color White to Light yellow
InChIInChI=1S/C6H4BrN3/c7-5-4-8-6-2-1-3-9-10(5)6/h1-4H
InChIKeyKJQVHOFAWISYDO-UHFFFAOYSA-N
SMILESC12=NC=C(Br)N1N=CC=C2
CAS DataBase Reference18087-73-5
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 24/25
HS Code 29339900
MSDS Information
3-BROMOIMIDAZO[1,2-B]PYRIDAZINE Usage And Synthesis
Uses3-Bromoimidazo[1,2-B]pyridazine is a pharmaceutical intermediate compound. It is used in the preparation of Ponatinib, a tyrosine kinase inhibitor (TKI), which is used in the treatment of chronic myeloid leukaemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukaemia (Ph+ ALL).
Synthesis
Imidazo[1,2-b]pyridazine

766-55-2

3-BROMOIMIDAZO[1,2-B]PYRIDAZINE

18087-73-5

Imidazo[1,2-b]pyridazine (6.0 g, 50.4 mmol) was used as starting material, and N-bromosuccinimide (NBS, 6.0 g, 75.6 mmol) and a catalytic amount of azobisisobutyronitrile (AIBN) were added in 50 mL of chloroform. The reaction mixture was heated and refluxed for 2 h, during which the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was cooled to room temperature and subsequently stirred under ice bath conditions to promote precipitation. The precipitate was separated by filtration and the filtrate was concentrated to afford the target product 3-bromoimidazo[1,2-b]pyridazine as a pale yellow solid in 75% yield.

References[1] Patent: CN105418615, 2016, A. Location in patent: Paragraph 0079 ; 0080 ; 0081; 0082; 0083; 0084
[2] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 23, p. 5830 - 5835
[3] Patent: EP2818471, 2014, A1. Location in patent: Paragraph 0122; 0123
[4] Synthesis, 1981, # 12, p. 987 - 989
[5] Patent: WO2016/210036, 2016, A1. Location in patent: Page/Page column 107
3-BROMOIMIDAZO[1,2-B]PYRIDAZINE Preparation Products And Raw materials
Raw materialsImidazo[1,2-b]pyridazine-->N-Bromosuccinimide-->ABIN-->Chloroform
Tag:3-BROMOIMIDAZO[1,2-B]PYRIDAZINE(18087-73-5) Related Product Information
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