tert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylate
97%
- Product Code: 46225
CAS:
164149-27-3
Molecular Weight: | 306.2392 g./mol | Molecular Formula: | C₁₃H₂₄BrNO₂ |
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EC Number: | MDL Number: | MFCD23701754 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of compounds with potential therapeutic applications. The presence of both the tert-butyl carboxylate group and the bromopropyl moiety allows for selective modifications, making it useful in constructing piperidine-based structures, which are common in drug discovery. Additionally, it can be employed in the preparation of ligands for catalysis or in the development of biologically active agents targeting neurological or metabolic disorders. Its reactive bromine atom facilitates further functionalization through cross-coupling reactions, enhancing its utility in medicinal chemistry and material science.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,818.00 |
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tert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of compounds with potential therapeutic applications. The presence of both the tert-butyl carboxylate group and the bromopropyl moiety allows for selective modifications, making it useful in constructing piperidine-based structures, which are common in drug discovery. Additionally, it can be employed in the preparation of ligands for catalysis or in the development of biologically active agents targeting neurological or metabolic disorders. Its reactive bromine atom facilitates further functionalization through cross-coupling reactions, enhancing its utility in medicinal chemistry and material science.
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