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2-Bromo-4-fluoronitrobenzene

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CAS:700-36-7
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Products Intro: Product Name:2-bromo-4-fluoro-1-nitrobenzene
CAS:700-36-7
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CAS:700-36-7
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Products Intro: Product Name:2-Bromo-4-fluoronitrobenzene
CAS:700-36-7
Purity:99% Package:1KG;1USD

2-Bromo-4-fluoronitrobenzene manufacturers

  • 2-Bromo-4-fluoronitrobenzene
  • 2-Bromo-4-fluoronitrobenzene pictures
  • $100.00 / 1KG
  • 2025-09-25
  • CAS:700-36-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
2-Bromo-4-fluoronitrobenzene Basic information
Product Name:2-Bromo-4-fluoronitrobenzene
Synonyms:2-bromo-4-fluoro-1-nitrobenzene;1-Bromo-5-fluoro-2-nitrobenzene;2-Bromo-4-fluoronitrobenzene;2-BroMo-4-fluoronitrobenzene, 97+%;2-Bromo-4-fluoro-1-nitrobenzene >;2-Bromo-4-fluoronitrobenzene,>98%;Benzene, 2-bromo-4-fluoro-1-nitro-;2-Bromo-4-fluoronitrobenzene ISO 9001:2015 REACH
CAS:700-36-7
MF:C6H3BrFNO2
MW:220
EINECS:670-950-4
Product Categories:
Mol File:700-36-7.mol
2-Bromo-4-fluoronitrobenzene Structure
2-Bromo-4-fluoronitrobenzene Chemical Properties
Melting point 44 °C
Boiling point 70-75 °C(Press: 0.4 Torr)
density 1.808±0.06 g/cm3(Predicted)
refractive index 1.57
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form Solid
color Pale yellow to green
InChIInChI=1S/C6H3BrFNO2/c7-5-3-4(8)1-2-6(5)9(10)11/h1-3H
InChIKeyVGYVBEJDXIPSDL-UHFFFAOYSA-N
SMILESC1([N+]([O-])=O)=CC=C(F)C=C1Br
CAS DataBase Reference700-36-7
Safety Information
Safety Statements 24/25
HS Code 29049090
MSDS Information
2-Bromo-4-fluoronitrobenzene Usage And Synthesis
Chemical PropertiesYellow to pale green powder
Uses2-Bromo-4-fluoro-1-nitrobenzene can be used as a valuable building block, mainly for the preparation of Benzimidazoles.
Synthesis
4-Fluoroaniline

371-40-4

2-Bromo-4-fluoronitrobenzene

700-36-7

General procedure for the synthesis of 1-bromo-5-fluoro-2-nitrobenzene from 4-fluoroaniline: N-bromosuccinimide (34 g, 180 mmol) was dissolved in dichloromethane (60 mL) at 0 °C and slowly added dropwise to a solution of 4-fluoroaniline (20 g, 180 mmol) in dichloromethane (100 mL). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, it was washed sequentially with saturated sodium sulfite solution, saturated sodium bicarbonate solution and brine, and then concentrated to give 1-bromo-5-fluoro-2-nitrobenzene (34 g, 154.5 mmol, 100% yield). The 1H NMR (400 MHz, CDCl3) data of the product were as follows: δ 7.12-7.21 (m, 1H), 7.47 (dd, J = 7.60, 2.40 Hz, 1H), (dd, J = 9.60, 6.40 Hz, 1H).

References[1] Patent: US2008/300242, 2008, A1. Location in patent: Page/Page column 62
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