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AA96004

180695-79-8 | 1-N-Boc-4-bromopiperidine

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.

Description
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

 

Computed Properties
Complexity: 205  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 2  
XLogP3: 2.4  

 

 

Upstream Synthesis Route
  • 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.
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