2-Iodobenzyl bromide

97%

  • Product Code: 123290
  Alias:    O-iodobenzyl bromide
  CAS:    40400-13-3
Molecular Weight: 296.93 g./mol Molecular Formula: IC₆H₄CH₂Br
EC Number: MDL Number: MFCD00236046
Melting Point: 54-60 °C(lit.) Boiling Point: 125 °C / 4mmHg
Density: Storage Condition: 2~8°C, away from light
Product Description: 2-Iodobenzyl bromide is primarily used in organic synthesis as a versatile building block for the preparation of various complex molecules. It is particularly valuable in the formation of carbon-carbon and carbon-heteroatom bonds through cross-coupling reactions, such as Suzuki and Heck reactions. The compound is also employed in the synthesis of pharmaceuticals, where it serves as an intermediate for the development of active pharmaceutical ingredients (APIs). Additionally, it finds application in the preparation of ligands for catalysis and in the construction of organic frameworks used in material science. Its reactivity with nucleophiles makes it a useful reagent for introducing the benzyl group into target molecules.
Product Specification:
Test Specification
Melting Point 52-58
Purity (GC) 97-100
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5
Purity (Titration By AgNO3 After O2 Combustion) 96.5-103.5
Appearance White To Tan Solid, Powder, Crystals And/Or Chunks
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $12.46
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5.000 10-20 days $37.79
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25.000 10-20 days $172.35
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2-Iodobenzyl bromide
2-Iodobenzyl bromide is primarily used in organic synthesis as a versatile building block for the preparation of various complex molecules. It is particularly valuable in the formation of carbon-carbon and carbon-heteroatom bonds through cross-coupling reactions, such as Suzuki and Heck reactions. The compound is also employed in the synthesis of pharmaceuticals, where it serves as an intermediate for the development of active pharmaceutical ingredients (APIs). Additionally, it finds application in the preparation of ligands for catalysis and in the construction of organic frameworks used in material science. Its reactivity with nucleophiles makes it a useful reagent for introducing the benzyl group into target molecules.
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