1-Bromo-4-heptanoylbenzene

98%

  • Product Code: 82207
  CAS:    99474-02-9
Molecular Weight: 269.19 g./mol Molecular Formula: C₁₃H₁₇BrO
EC Number: MDL Number: MFCD00276567
Melting Point: 69-72 °C Boiling Point:
Density: Storage Condition: room temperature, sealed
Product Description: 1-Bromo-4-heptanoylbenzene is primarily used in organic synthesis as an intermediate for the preparation of various complex molecules. Its structure, featuring both a bromo and a heptanoyl group, makes it a versatile building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create carbon-carbon bonds, which are essential in constructing larger organic frameworks. Additionally, it serves as a precursor in the synthesis of liquid crystals and other advanced materials, where its aromatic and aliphatic components contribute to desired properties like stability and solubility. Its applications also extend to research and development, where it is used to explore new synthetic pathways and chemical transformations.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿4,275.00
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1-Bromo-4-heptanoylbenzene
1-Bromo-4-heptanoylbenzene is primarily used in organic synthesis as an intermediate for the preparation of various complex molecules. Its structure, featuring both a bromo and a heptanoyl group, makes it a versatile building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create carbon-carbon bonds, which are essential in constructing larger organic frameworks. Additionally, it serves as a precursor in the synthesis of liquid crystals and other advanced materials, where its aromatic and aliphatic components contribute to desired properties like stability and solubility. Its applications also extend to research and development, where it is used to explore new synthetic pathways and chemical transformations.
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