2-Fluoro-4-Iodophenol

2-Fluoro-4-Iodophenol Suppliers list
Company Name: Shaanxi Didu New Material Co., Ltd
Tel: 81124267 17392282731
Email: 1073@dideu.com
Products Intro: Product Name:2-Fluoro-4-Iodophenol
CAS:2713-28-2
Purity:99% HPLC Package:5KG;1KG
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718 +86-13336195806
Email: sales@capot.com
Products Intro: Product Name:2-Fluoro-4-iodophenol
CAS:2713-28-2
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Win-Win Chemical CO., Limited
Tel: 0086-577-64498589
Email: sales@win-winchemical.com
Products Intro: Product Name:2-Fluoro-4-Iodophenol
CAS:2713-28-2
Purity:98% Package:100g:1kg:10kg Remarks:pharmaceutical intermediates
Company Name: Changzhou Ansciep Chemical Co., Ltd.
Tel: +86 519 86305871
Email: sales@ansciepchem.com
Products Intro: Product Name:2-Fluoro-4-iodophenol
CAS:2713-28-2
Purity:0.99 Package:100g, 500g, 1kg, 25kg, 50kg, 200kg Remarks:Good quality; Large stock; Hot sale
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322
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Products Intro: Product Name:2-Fluoro-4-iodophenol
CAS:2713-28-2
Purity:>97% Package:1g;5g;10g;25g;100g Remarks:SY065736

2-Fluoro-4-Iodophenol manufacturers

2-Fluoro-4-Iodophenol Basic information
Product Name:2-Fluoro-4-Iodophenol
Synonyms:Phenol,2-fluoro-4-iodo-;4-Iodo-2-fluorophenol;2-Fluoro-4-Iodophenol;O-Fluoro-P-Iodophenol;2-Fluoro-4-Iodopheno;4-iodine-2-fluorophenol
CAS:2713-28-2
MF:C6H4FIO
MW:238
EINECS:
Product Categories:
Mol File:Mol File
2-Fluoro-4-Iodophenol Structure
2-Fluoro-4-Iodophenol Chemical Properties
Boiling point 238.1±25.0 °C(Predicted)
density 2.085±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Store in freezer, under -20°C
pka8.10±0.18(Predicted)
form solid
color Light yellow to yellow
Safety Information
HS Code 2908190090
MSDS Information
2-Fluoro-4-Iodophenol Usage And Synthesis
Synthesis
2-Fluorophenol

367-12-4

2-Fluoro-4-Iodophenol

2713-28-2

General procedure for the synthesis of 2-fluoro-4-iodophenol from 2-fluorophenol: Iodine (1.06 g, 4.18 mmol) was added in a single addition to a stirring solution of 2-fluorophenol (0.47 g, 4.18 mmol) in concentrated ammonia (22 ml) at room temperature. The reaction mixture was stirred overnight at room temperature and the solvent was removed by evaporation under reduced pressure. The residue was partitioned between ethyl acetate (100 ml) and water (40 ml). The organic phase was washed sequentially with 5% sodium bisulfite solution and brine (10 ml), dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate, 9:1) to afford 2-fluoro-4-iodophenol (0.42 g, 42% yield) as a colorless solid.1H-NMR (CDCl3) δ 7.3-7.4 (m, 2H), 6.75 (t, J=8.8 Hz, 1H), 5.17 (s, 1H).

References[1] Tetrahedron Letters, 2010, vol. 51, # 16, p. 2170 - 2173
[2] Patent: WO2014/63199, 2014, A1. Location in patent: Page/Page column 94
[3] Canadian Journal of Chemistry, 1965, vol. 43, p. 650 - 658
[4] Patent: EP409634, 1991, A2
2-Fluoro-4-Iodophenol Preparation Products And Raw materials
Raw materials2-Fluorophenol
Preparation Products3-(3-fluoro-4-hydroxyphenyl)acrylic acid
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