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3-Chloro-6-iodopyridazine

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CAS:135034-10-5
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  • 3-Chloro-6-iodopyridazine
  • 3-Chloro-6-iodopyridazine pictures
  • $200.00 / 1KG
  • 2025-09-25
  • CAS:135034-10-5
  • Min. Order: 1KG
  • Purity: 99%
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3-Chloro-6-iodopyridazine Basic information
Product Name:3-Chloro-6-iodopyridazine
Synonyms:3-Chloro-6-pyrazine;3-Chloro-6-iodopyridazine;Pyridazine, 3-chloro-6-iodo-;3-Chloro-6-iodo-1,2-diazine;3-Chloro-6-iodopyridazine Pyridazine, 3-chloro-6-iodo-;3-Chloro-6-iodopyridazine,97%;3-Chloro-6-iodopyridazine ISO 9001:2015 REACH;SWF-116
CAS:135034-10-5
MF:C4H2ClIN2
MW:240.43
EINECS:
Product Categories:Halides;Pyrazines, Pyrimidines & Pyridazines;Pyrazines, Pyrimidines & Pyridazines;Heterocyclic Building Blocks
Mol File:135034-10-5.mol
3-Chloro-6-iodopyridazine Structure
3-Chloro-6-iodopyridazine Chemical Properties
Melting point 118-120°
Boiling point 327.7±22.0 °C(Predicted)
density 2.187±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka-1.18±0.10(Predicted)
form Solid
AppearanceWhite to light brown Solid
Water Solubility Slightly soluble in water.
InChIInChI=1S/C4H2ClIN2/c5-3-1-2-4(6)8-7-3/h1-2H
InChIKeyPNEPCDPKMXJYIQ-UHFFFAOYSA-N
SMILESC1(Cl)=NN=C(I)C=C1
Safety Information
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 2933998090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
3-Chloro-6-iodopyridazine Usage And Synthesis
Uses3-Chloro-6-iodopyridazine is a reactant in the Suzuki-Miyaura coupling reaction as well as a reactant in the synthesis of 6-Chloropyridazine-3-carbonitrile (C368635).
Synthesis
3,6-Dichloropyridazine

141-30-0

3-Chloro-6-iodopyridazine

135034-10-5

The general procedure for the synthesis of 3-chloro-6-iodopyridazine from 3,6-dichloropyridazine was as follows: the intermediate (E)-3-{3-[3'-(1-adamantyl)-4'-hydroxyphenyl]-6-pyridazinyl}-2-propenoic acid ethyl ester was prepared as follows. a) Synthesis of 3-chloro-6-iodopyridazine. Followed the method reported in the literature (Goodman, A.J. et al., Tetrahedron, 1999, 55, 15067-15070). A suspension of 3,6-dichloropyridazine (5.000 g, 33.56 mmol), NaI (6.75 g, 45.0 mmol), and HI (55% to 58%, 25 mL) was stirred for 23 h at 44 °C (oil bath) under argon protection. After completion of the reaction, the mixture was cooled to room temperature and quenched with concentrated HCl. Subsequently, the pH was adjusted to 12 with NaOH, stirred for 10 min and extracted with CH2Cl2. The organic phase was washed with water and dried. The solvent was removed under reduced pressure to give 7.96 g (98% yield) of 3-chloro-6-iodopyridazine as a light yellow solid with a melting point of 114-116 °C (literature value: 110-112 °C). 1H NMR (CDCl3) δ 7.23 (d, J = 8.7 Hz, 1H, 4-ArH), 7.84 ppm (d, J = 8.7 Hz, 1H, 5-ArH).

References[1] Patent: US2010/4443, 2010, A1. Location in patent: Page/Page column 34
[2] Patent: WO2011/79305, 2011, A1. Location in patent: Page/Page column 41
[3] Journal of Medicinal Chemistry, 2011, vol. 54, # 11, p. 3793 - 3816
[4] Tetrahedron, 1999, vol. 55, # 52, p. 15067 - 15070
[5] Patent: US2005/234046, 2005, A1. Location in patent: Page/Page column 66
3-Chloro-6-iodopyridazine Preparation Products And Raw materials
Raw materials3,6-Dichloropyridazine-->Sodium hydroxide-->Hydriodic acid-->Sodium iodide
Preparation Products3-Chloro-6-trifluoromethyl-pyridazine-->3-Chloro-6-(4-fluorophenyl)pyridazine
Tag:3-Chloro-6-iodopyridazine(135034-10-5) Related Product Information
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