Cas no 2803859-63-2 (1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate)

1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate is a cyclobutyl-substituted piperidine derivative featuring a tert-butoxycarbonyl (Boc) protecting group and a bromine substituent on the cyclobutyl ring. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmacologically active molecules. The Boc group enhances stability and facilitates selective deprotection under mild acidic conditions, while the bromine moiety offers a reactive site for further functionalization via cross-coupling or nucleophilic substitution reactions. Its rigid cyclobutyl structure can contribute to conformational constraint in target molecules, potentially improving binding affinity in drug discovery applications. The compound is typically handled under inert conditions due to the reactivity of the bromine substituent.
1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate structure
2803859-63-2 structure
Product Name:1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate
CAS No:2803859-63-2
MF:C14H24BrNO2
MW:318.249863624573
CID:5863026
Update Time:2025-06-09

1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate Chemical and Physical Properties

Names and Identifiers

    • 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate
    • Inchi: 1S/C14H24BrNO2/c1-14(2,3)18-13(17)16-6-4-10(5-7-16)11-8-12(15)9-11/h10-12H,4-9H2,1-3H3
    • InChI Key: DJZRGGXNFQKBPB-UHFFFAOYSA-N
    • SMILES: N1(C(OC(C)(C)C)=O)CCC(C2CC(Br)C2)CC1

Experimental Properties

  • Density: 1.305±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
  • Boiling Point: 362.2±42.0 °C(Predicted)
  • pka: -1.33±0.40(Predicted)

1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate Pricemore >>

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Additional information on 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate

Research Brief on 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate (CAS: 2803859-63-2)

1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate (CAS: 2803859-63-2) is a specialized chemical compound that has recently garnered attention in the field of chemical biology and pharmaceutical research. This compound, characterized by its unique cyclobutyl and piperidine moieties, serves as a critical intermediate in the synthesis of novel bioactive molecules. Recent studies have explored its potential applications in drug discovery, particularly in the development of small-molecule inhibitors targeting various disease pathways.

The compound's structural features, including the bromocyclobutyl group, make it a versatile building block for medicinal chemistry. Researchers have utilized it in the synthesis of compounds with potential therapeutic effects, such as kinase inhibitors and modulators of G-protein-coupled receptors (GPCRs). Its role in facilitating the construction of complex molecular architectures has been highlighted in several recent publications, underscoring its importance in modern drug development.

One of the key areas of investigation has been the optimization of synthetic routes for 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate. Recent advancements in catalytic methods and green chemistry have enabled more efficient and scalable production of this compound, addressing previous challenges related to yield and purity. These improvements are critical for its broader application in high-throughput screening and lead optimization processes.

In addition to its synthetic utility, the compound has been studied for its biological activity. Preliminary in vitro assays suggest that derivatives of 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate exhibit promising activity against certain cancer cell lines and inflammatory targets. These findings have spurred further research into its mechanism of action and potential as a scaffold for drug candidates.

Looking ahead, the continued exploration of 1,1-Dimethylethyl 4-(3-bromocyclobutyl)-1-piperidinecarboxylate and its derivatives is expected to yield significant insights into its therapeutic potential. Collaborative efforts between academic and industrial researchers are likely to accelerate the translation of these discoveries into clinical applications, paving the way for new treatments in oncology, immunology, and beyond.

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