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2-FLUORORESORCINOL

2-FLUORORESORCINOL Suppliers list
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718; +8613336195806
Email: sales@capot.com
Products Intro: Product Name:2-Fluororesorcinol
CAS:103068-40-2
Purity:98%(Min,GC) Package:1G;1KG;100KG
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
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Products Intro: Product Name:2-Fluorobenzene-1,3-diol
CAS:103068-40-2
Remarks:MG25032
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: factory@coreychem.com
Products Intro: Product Name:2-Fluoro-1,3-benzenediol
CAS:103068-40-2
Purity:>98%HPLC Package:1KG;9.8USD
Company Name: Fuxin Pharmaceutical
Tel: +86-021-021-50872116 +8613122107989
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Products Intro: Product Name:2-Fluorobenzene-1,3-diol
CAS:103068-40-2
Purity:99% Package:1kg; 25kg; or larger package as required
Company Name: SHANGHAI T&W PHARMACEUTICAL CO., LTD.
Tel: +86-021-61551413 +8618813727289
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Products Intro: Product Name:2-FLUORORESORCINOL
CAS:103068-40-2

2-FLUORORESORCINOL manufacturers

2-FLUORORESORCINOL Basic information
Product Name:2-FLUORORESORCINOL
Synonyms:2-fluororesocinol;2-Fluoro-1,3-benzenediol;1,3-Benzenediol, 2-fluoro-;2-fluoro-1,3-dihydroxybenzene;2-Fluoro-1,3-diol
CAS:103068-40-2
MF:C6H5FO2
MW:128.1
EINECS:
Product Categories:
Mol File:103068-40-2.mol
2-FLUORORESORCINOL Structure
2-FLUORORESORCINOL Chemical Properties
Melting point 114-116 °C
Boiling point 223.5±20.0 °C(Predicted)
density 1.415±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka8.19±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2908990000
MSDS Information
2-FLUORORESORCINOL Usage And Synthesis
Synthesis
2-fluoro-3-Methoxyphenol

447462-87-5

2-FLUORORESORCINOL

103068-40-2

General procedure for the demethylation of BBr3: 2-fluoro-3-methoxyphenol (8.7 mmol) was dissolved in dry dichloromethane (40 mL) under nitrogen protection and cooled to -78°C. BBr3 (1 M solution in dichloromethane, 4 equivalents per methoxide) was added slowly and dropwise. The reaction mixture was stirred at -78 °C overnight, during which time the cooling bath was allowed to warm naturally to room temperature. Upon completion of the reaction, the mixture was cooled again to -78 °C and the reaction was quenched by careful dropwise addition of water. The aqueous layer was extracted with EtOAc, the organic layers were combined and dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure to give the crude product. The crude product was ground with EtOAc to give 2-fluoro-1,3-benzenediol, which could be used in subsequent reactions without further purification. The yield of the method was 93%. Mass spectrometry (MS) data: m/z 129.1 (MH+).

References[1] Patent: US2009/298820, 2009, A1. Location in patent: Page/Page column 34
[2] Patent: WO2010/30727, 2010, A1. Location in patent: Page/Page column 92-93
[3] Patent: EP3401309, 2018, A1. Location in patent: Paragraph 0505
[4] Patent: US2009/311217, 2009, A1. Location in patent: Page/Page column 51
[5] Patent: WO2006/57860, 2006, A1. Location in patent: Page/Page column 114-115
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