4-Bromobenzonitrile

98%

  • Product Code: 119408
  Alias:    4-bromocyanobenzene; p-bromobenzonitrile; p-bromobenzonitrile; p-bromocyanobenzene; 4-bromobenzonitrile; 4-bromobenzonitrile;
  CAS:    623-00-7
Molecular Weight: 182.02 g./mol Molecular Formula: C₇H₄BrN
EC Number: MDL Number: MFCD00001811
Melting Point: 110-115 °C(lit.) Boiling Point: 235-237 °C(lit.)
Density: Storage Condition: room temperature
Product Description: Used primarily in organic synthesis, 4-Bromobenzonitrile serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it valuable in constructing complex organic molecules. It is also employed in the development of liquid crystals and electronic materials due to its aromatic and nitrile functional groups, which contribute to stability and polarity. Additionally, it finds use in research for studying reaction mechanisms and developing new synthetic pathways.
Product Specification:
Test Specification
Carbon 45.4-45.8
Nitrogen 7.5-7.9
Purity (%) 97.5-100
Melting Point 111-114
Appearance WHITE TO LIGHT YELLOW POWDER OR CRYSTALS
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿290.00
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25.000 10-20 days ฿660.00
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100.000 10-20 days ฿2,280.00
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500.000 10-20 days ฿10,870.00
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4-Bromobenzonitrile
Used primarily in organic synthesis, 4-Bromobenzonitrile serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it valuable in constructing complex organic molecules. It is also employed in the development of liquid crystals and electronic materials due to its aromatic and nitrile functional groups, which contribute to stability and polarity. Additionally, it finds use in research for studying reaction mechanisms and developing new synthetic pathways.
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