2-Bromoiodobenzene

98%, with stabilizer copper shavings

  • Product Code: 123261
  Alias:    o-bromoiodobenzene; 1-bromo-2-iodobenzene, 2-iodobenzonitrile
  CAS:    583-55-1
Molecular Weight: 282.9 g./mol Molecular Formula: BrC₆H₄I
EC Number: 209-508-9 MDL Number: MFCD00001030
Melting Point: 9-10 °C(lit.) Boiling Point: 120-121 °C15 mm Hg(lit.)
Density: 2.203 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: 2-Bromoiodobenzene is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is commonly employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to form carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its dual halogen functionality allows for selective reactivity, enabling chemists to introduce specific structural motifs into target compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds and functionalized aromatic systems, which are valuable in drug discovery and material science. Its stability and reactivity make it a useful reagent in both academic research and industrial applications.
Product Specification:
Test Specification
Purity (GC) 98-100
Refractive Index N20/D 1.6625-1.6675
Appearance Colorless To Yellow Liquid
Infrared Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿290.00
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5.000 10-20 days ฿410.00
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25.000 10-20 days ฿660.00
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100.000 10-20 days ฿2,600.00
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500.000 10-20 days ฿12,880.00
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2-Bromoiodobenzene
2-Bromoiodobenzene is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is commonly employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to form carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its dual halogen functionality allows for selective reactivity, enabling chemists to introduce specific structural motifs into target compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds and functionalized aromatic systems, which are valuable in drug discovery and material science. Its stability and reactivity make it a useful reagent in both academic research and industrial applications.
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