N-Boc-1-(bromomethyl)cyclopropanamine

≥95%

  • Product Code: 68166
  CAS:    387845-49-0
Molecular Weight: 250.13 g./mol Molecular Formula: C₉H₁₆BrNO₂
EC Number: MDL Number: MFCD23701521
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This compound is primarily used in organic synthesis as a versatile building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of cyclopropane-containing drugs, where the cyclopropane ring can enhance biological activity or stability. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine, allowing selective reactions to occur at other sites of the molecule. The bromomethyl group provides a reactive site for further functionalization, such as nucleophilic substitution or cross-coupling reactions. This makes it a useful intermediate in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it can be employed in the creation of peptidomimetics or other small molecules for medicinal chemistry research.
Product Specification:
Test Specification
APPEARANCE White to yellow solid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿10,125.00
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-
1.000 10-20 days ฿24,111.00
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-
5.000 10-20 days ฿67,500.00
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N-Boc-1-(bromomethyl)cyclopropanamine
This compound is primarily used in organic synthesis as a versatile building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of cyclopropane-containing drugs, where the cyclopropane ring can enhance biological activity or stability. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine, allowing selective reactions to occur at other sites of the molecule. The bromomethyl group provides a reactive site for further functionalization, such as nucleophilic substitution or cross-coupling reactions. This makes it a useful intermediate in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it can be employed in the creation of peptidomimetics or other small molecules for medicinal chemistry research.
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