tert-Butyl 6-bromo-4H-spiro[benzo[d][1,3]-dioxine-2,4'-piperidine]-1'-carboxylate

95%

  • Product Code: 75729
  CAS:    895525-73-2
Molecular Weight: 384.28 g./mol Molecular Formula: C₁₇H₂₂BrNO₄
EC Number: MDL Number: MFCD13195393
Melting Point: Boiling Point: 474.441℃ at 760 mmHg
Density: 1.434 g/ml Storage Condition: 2-8°C, dry, sealed
Product Description: This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. The spirocyclic structure and functional groups present in the molecule make it valuable for constructing diverse chemical architectures, especially in the design of central nervous system (CNS) targeting drugs. It is also employed in medicinal chemistry for exploring structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Additionally, its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of novel derivatives for biological evaluation.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $335.64
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1.000 10-20 days $672.02
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tert-Butyl 6-bromo-4H-spiro[benzo[d][1,3]-dioxine-2,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. The spirocyclic structure and functional groups present in the molecule make it valuable for constructing diverse chemical architectures, especially in the design of central nervous system (CNS) targeting drugs. It is also employed in medicinal chemistry for exploring structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Additionally, its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of novel derivatives for biological evaluation.
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