5-Bromo-3-iodo-1H-indazole

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5-Bromo-3-iodo-1H-indazole manufacturers

  • 5-BROMO-3-IODO (1H)INDAZOLE
  • 5-BROMO-3-IODO (1H)INDAZOLE pictures
  • $15.00 / 1KG
  • 2021-07-13
  • CAS:459133-66-5
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
  • 5-BROMO-3-IODO (1H)INDAZOLE
  • 5-BROMO-3-IODO (1H)INDAZOLE pictures
  • $15.00 / 1KG
  • 2021-07-10
  • CAS:459133-66-5
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
5-Bromo-3-iodo-1H-indazole Basic information
Product Name:5-Bromo-3-iodo-1H-indazole
Synonyms:1H-Indazole, 5-broMo-3-iodo--3;5-BROMO-3-IODO (1H)INDAZOLE;5-BROMO-3-IODOINDAZOLE;1H-Indazole, 5-broMo-3-iodo--
CAS:459133-66-5
MF:C7H4BrIN2
MW:322.93
EINECS:200-258-5
Product Categories:
Mol File:459133-66-5.mol
5-Bromo-3-iodo-1H-indazole Structure
5-Bromo-3-iodo-1H-indazole Chemical Properties
Melting point 196 °C(Solv: ligroine (8032-32-4))
Boiling point 413.1±25.0 °C(Predicted)
density 2.421±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.78±0.40(Predicted)
AppearanceOff-white to light yellow Solid
InChIInChI=1S/C7H4BrIN2/c8-4-1-2-6-5(3-4)7(9)11-10-6/h1-3H,(H,10,11)
InChIKeyIBFAYUXCRDDBRD-UHFFFAOYSA-N
SMILESN1C2=C(C=C(Br)C=C2)C(I)=N1
Safety Information
RIDADR UN2811
HS Code 2933998090
MSDS Information
5-Bromo-3-iodo-1H-indazole Usage And Synthesis
Uses5-Bromo-3-iodo-1H-indazole is important chemical intermediate.
Synthesis
5-bromo-1H-indazole

53857-57-1

5-Bromo-3-iodo-1H-indazole

459133-66-5

General procedure for the synthesis of 5-bromo-3-iodo-1H-indazole from 5-bromo-1H-indazole: To a solution of 5-bromo-1H-indazole (5.0 g, 25.4 mmol, 1.0 eq.) in anhydrous DMF (15.0 mL) was added sequentially, protected by nitrogen, KOH (4.3 g, 76.1 mmol, 3.0 eq.) and iodine (12.9 g, 50.75 mmol, 2.0 equiv). The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction solution was diluted with ice water and then extracted with ethyl acetate (50 mL x 2). The organic layers were combined, washed sequentially with aqueous Na2S2O3 and brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to afford the crude product 5-bromo-3-iodo-1H-indazole (8.0 g, 97.9% yield), which could be used for the next reaction without further purification.

References[1] Molecules, 2018, vol. 23, # 8,
[2] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2361 - 2372
[3] Patent: WO2017/98328, 2017, A2. Location in patent: Paragraph 00213
[4] Synthesis, 2006, # 20, p. 3506 - 3514
[5] Letters in Drug Design and Discovery, 2013, vol. 10, # 7, p. 625 - 631
5-Bromo-3-iodo-1H-indazole Preparation Products And Raw materials
Raw materials5-bromo-1H-indazole-->Potassium hydroxide-->iodine-->N,N-Dimethylformamide
Preparation Products5-BroMo-3-(Methylthio)-1H-indazole
Tag:5-Bromo-3-iodo-1H-indazole(459133-66-5) Related Product Information
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