AA96004
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $8.00 | $5.00 | - + | |
1g | 98% | in stock | $12.00 | $8.00 | - + | |
5g | 98% | in stock | $15.00 | $10.00 | - + | |
10g | 98% | in stock | $25.00 | $17.00 | - + | |
25g | 98% | in stock | $58.00 | $40.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA96004 |
Chemical Name: | 1-N-Boc-4-bromopiperidine |
CAS Number: | 180695-79-8 |
Molecular Formula: | C10H18BrNO2 |
Molecular Weight: | 264.1594 |
MDL Number: | MFCD04115039 |
SMILES: | BrC1CCN(CC1)C(=O)OC(C)(C)C |
Complexity: | 205 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 2 |
XLogP3: | 2.4 |
N-Boc-4-Bromopiperidine is a versatile compound that finds significant applications in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique properties and reactivity. When utilized in synthesis, N-Boc-4-Bromopiperidine can act as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and other complex organic molecules.One of the primary uses of N-Boc-4-Bromopiperidine is in the synthesis of pharmaceutical drugs. By incorporating this compound into the chemical structure of a target molecule, chemists can modify the biological activity, solubility, or stability of the final drug product. Additionally, the presence of the Boc (tert-butoxycarbonyl) protecting group in N-Boc-4-Bromopiperidine allows for selective functionalization of specific positions within the molecule, enabling precise control over the synthetic pathway.Moreover, N-Boc-4-Bromopiperidine can participate in various organic reactions such as nucleophilic substitution, palladium-catalyzed cross-coupling, and reductive amination, expanding its synthetic utility in the preparation of diverse chemical compounds. The bromine atom present in the structure provides a handle for further derivatization, facilitating the introduction of additional functional groups for fine-tuning the properties of the final product.In conclusion, the strategic incorporation of N-Boc-4-Bromopiperidine in chemical synthesis enables chemists to access a wide range of structurally diverse compounds with tailored properties. This versatile building block plays a vital role in the design and development of new molecules for applications in the pharmaceutical, agrochemical, and materials science industries.