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2-Bromo-3-fluoronitrobenzene

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Company Name: Hebei Mojin Biotechnology Co., Ltd
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Products Intro: Product Name:2-Bromo-3-fluoronitrobenzene
CAS:59255-94-6
Purity:99% Package:25KG
Company Name: Hebei Xinsheng New Material Technology Co., LTD.
Tel: +86-16632316109
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Products Intro: Product Name:2-Bromo-3-fluoronitrobenzene
CAS:59255-94-6
Purity:99% Package:1kg;35USD|100kg;30USD|1000kg;25USD
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Products Intro: Product Name:2-Bromo-1-fluoro-3-nitrobenzene
CAS:59255-94-6
Purity:98%(Min,GC) Package:1G;1KG;100KG
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Products Intro: CAS:59255-94-6
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G
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Products Intro: Product Name:2-Bromo-3-fluoronitrobenzene
CAS:59255-94-6
Purity:99% Package:1KG;1USD

2-Bromo-3-fluoronitrobenzene manufacturers

2-Bromo-3-fluoronitrobenzene Basic information
Product Name:2-Bromo-3-fluoronitrobenzene
Synonyms:2-BROMO-3-FLUORONITROBENZENE;2-broMo-3-fluorobroMobezene;Benzene, 2-bromo-1-fluoro-3-nitro-;2-Bromo-3-fluoronitrobenzene ISO 9001:2015 REACH;2-Bromo-1-fluoro-3-nitrobenzene;1-Bromo-2-fluoro-6-nitrobenzene
CAS:59255-94-6
MF:C6H3BrFNO2
MW:220
EINECS:1533716-785-6
Product Categories:blocks;Bromides;FluoroCompounds;NitroCompounds
Mol File:59255-94-6.mol
2-Bromo-3-fluoronitrobenzene Structure
2-Bromo-3-fluoronitrobenzene Chemical Properties
Melting point 42.0-44.0 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
Boiling point 222.3±20.0 °C(Predicted)
density 1.808±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
color yellow
CAS DataBase Reference59255-94-6(CAS DataBase Reference)
Safety Information
Hazard Codes T
HazardClass IRRITANT
HS Code 2904990090
MSDS Information
2-Bromo-3-fluoronitrobenzene Usage And Synthesis
SynthesisPreparation method of 2-bromo-3-fluoronitrobenzene: Add 21.6g (0.1mol) 2-bromo-3-nitroaniline, 12.5ml (0.15mol) concentrated hydrochloric acid, and 12.5ml water into a reaction bottle, and reduce the temperature to 15°C; dissolve 8.3g (0.12mol) sodium nitrite in 14.5ml water and slowly add dropwise to the above system, then add 11.4g (0.13mol) fluoroboric acid, keep warm at 15°C and stir for 2 hours, track the reaction by HPLC until the reaction of 2-bromo-3-nitroaniline is complete; filter, rinse the filter cake with methanol, and dry to obtain 25.8g of intermediate IV. Add 30 ml of toluene to the reaction flask, heat to 100 ° C, slowly add 10 g (31.7 mmol) of intermediate IV, keep warm and stir for 1 hour, track the reaction by HPLC until the intermediate IV reacts completely: concentrate, recrystallize from ethyl acetate and n-hexane to obtain 5.7 g of 2-Bromo-3-fluoronitrobenzene, with a molar yield of 83%.2-Bromo-3-fluoronitrobenzene
2-Bromo-3-fluoronitrobenzene Preparation Products And Raw materials
Preparation Products1-BROMO-4-FLUORO-2-NITROBENZENE-->2-Bromo-3-fluoroaniline-->3-fluoro-2-(tetrahydrofuran-2-yl)aniline
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