1-Adamantyl bromomethyl ketone

97%

  • Product Code: 76952
  CAS:    5122-82-7
Molecular Weight: 257.17 g./mol Molecular Formula: C₁₂H₁₇BrO
EC Number: MDL Number: MFCD00074740
Melting Point: 76-79 °C (lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: 1-Adamantyl bromomethyl ketone is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its adamantyl group provides steric bulk and stability, making it valuable in the development of pharmaceuticals, particularly in the synthesis of antiviral and antibacterial agents. The bromomethyl moiety allows for further functionalization, enabling the creation of derivatives with potential biological activity. Additionally, it is employed in materials science for the design of advanced polymers and coatings, where its unique structure contributes to enhanced thermal and chemical resistance. Researchers also explore its use in the development of novel catalysts and ligands for asymmetric synthesis, leveraging its rigid framework to influence stereochemical outcomes.
Product Specification:
Test Specification
APPEARANCE White Crystalline powder
PURITY 96.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $79.36
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5.000 10-20 days $319.94
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1-Adamantyl bromomethyl ketone
1-Adamantyl bromomethyl ketone is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its adamantyl group provides steric bulk and stability, making it valuable in the development of pharmaceuticals, particularly in the synthesis of antiviral and antibacterial agents. The bromomethyl moiety allows for further functionalization, enabling the creation of derivatives with potential biological activity. Additionally, it is employed in materials science for the design of advanced polymers and coatings, where its unique structure contributes to enhanced thermal and chemical resistance. Researchers also explore its use in the development of novel catalysts and ligands for asymmetric synthesis, leveraging its rigid framework to influence stereochemical outcomes.
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