2-Fluoro-4-Iodophenol

2-Fluoro-4-Iodophenol Suppliers list
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn
Company Name: Nanjing JinruiJiuAn Biotechnology Co., Ltd.  
Tel: 025-58196018 800028039
Email: sales@fartop.net
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: 021-58170097
Email: info@topbiochem.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: +86-21-60341587
Email: sales@topbiochem.com

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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