1-N-Boc-3-(4-Bromophenoxy)pyrrolidine
97%
- Product Code: 114560
CAS:
1159825-42-9
Molecular Weight: | 342.23 g./mol | Molecular Formula: | C₁₅H₂₀BrNO₃ |
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EC Number: | MDL Number: | MFCD12068410 | |
Melting Point: | Boiling Point: | 403.6±35.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of complex molecules, especially those involving pyrrolidine derivatives. The Boc (tert-butoxycarbonyl) group provides protection for the amine functionality during multi-step synthetic processes, allowing for selective reactions at other sites of the molecule. The presence of the 4-bromophenoxy moiety makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing advanced drug candidates. Its application is particularly significant in the synthesis of compounds targeting neurological disorders, cancer, and other therapeutic areas.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,278.00 |
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0.250 | 10-20 days | ฿2,025.00 |
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1.000 | 10-20 days | ฿5,193.00 |
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1-N-Boc-3-(4-Bromophenoxy)pyrrolidine
This chemical is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of complex molecules, especially those involving pyrrolidine derivatives. The Boc (tert-butoxycarbonyl) group provides protection for the amine functionality during multi-step synthetic processes, allowing for selective reactions at other sites of the molecule. The presence of the 4-bromophenoxy moiety makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing advanced drug candidates. Its application is particularly significant in the synthesis of compounds targeting neurological disorders, cancer, and other therapeutic areas.
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