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2,6-Difluoroiodobenzene

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CAS:13697-89-7
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  • 2,6-Difluoroiodobenzene
  • 2,6-Difluoroiodobenzene pictures
  • $101.00 / 1KG
  • 2025-09-25
  • CAS:13697-89-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
2,6-Difluoroiodobenzene Basic information
Product Name:2,6-Difluoroiodobenzene
Synonyms:2,6-DIFLUORO-1-IODOBENZENE;2-Iodo-1,3-difluorobenzene;Benzene,1,3-difluoro-2-iodo-;1,3-Difluoro-2-iodobenzene>;2,6-Difluoroiodobenzene ISO 9001:2015 REACH
CAS:13697-89-7
MF:C6H3F2I
MW:239.99
EINECS:
Product Categories:Aromatic Hydrocarbons (substituted) & Derivatives;Fluorine Compounds;Iodine Compounds
Mol File:13697-89-7.mol
2,6-Difluoroiodobenzene Structure
2,6-Difluoroiodobenzene Chemical Properties
Melting point 24-26℃
Boiling point 186℃
density 2.001
Fp 69℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to lump to clear liquid
color White or Colorless to Yellow
InChIKeyVQMXWPLTZBKNEH-UHFFFAOYSA-N
CAS DataBase Reference13697-89-7
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 2903998090
MSDS Information
2,6-Difluoroiodobenzene Usage And Synthesis
Synthesis
1,3-Difluorobenzene

372-18-9

2,6-Difluoroiodobenzene

13697-89-7

The general procedure for the synthesis of 2,6-difluoroiodobenzene from 1,3-difluorobenzene was as follows: n-butyllithium (n-BuLi, 42 mL, 105 mmol) was slowly added to an anhydrous tetrahydrofuran (THF, 50 mL) solution of 1,3-difluorobenzene (10.0 g, 87 mmol) over a period of 10 min at -78 °C and under nitrogen protection. Subsequently, the reaction mixture was gradually warmed to room temperature and held for 5 minutes. Next, a tetrahydrofuran (THF, 200 mL) solution of iodine (26.7 g, 105 mmol) was slowly added and the reaction mixture continued to be stirred for 4 hours at room temperature. Upon completion of the reaction, the reaction was quenched with water and the organic phase was extracted with dichloromethane (CH2Cl2), followed by washing the organic layer with brine and drying with anhydrous sodium sulfate (Na2SO4). After filtration, the target product 2,6-difluoroiodobenzene (12.5 g, 74% yield) was obtained by concentration under reduced pressure. The structure of the product was confirmed by 1H NMR (CDCl3): δ 7.24-7.30 (1H, m), 6.89 (2H, dd, J = 6.6 Hz, 8.4 Hz).

References[1] European Journal of Organic Chemistry, 2002, # 19, p. 3351 - 3358
[2] Angewandte Chemie - International Edition, 2018, vol. 57, # 1, p. 187 - 191
[3] Angew. Chem., 2018, vol. 130, p. 193 - 197,5
[4] Patent: WO2013/71865, 2013, A1. Location in patent: Page/Page column 56
[5] Patent: CN103102349, 2017, B. Location in patent: Paragraph 0493-0495
2,6-Difluoroiodobenzene Preparation Products And Raw materials
Raw materials1,3-Difluorobenzene-->iodine-->n-Butyllithium-->Tetrahydrofuran
Preparation ProductsIodoacetonitrile
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