1'-Boc-5-Bromo-1,2-dihydro-2-oxo-spiro[3H-indole-3,4'-piperidine]

95%

  • Product Code: 66054
  CAS:    873779-30-7
Molecular Weight: 381.28 g./mol Molecular Formula: C₁₇H₂₁BrN₂O₃
EC Number: MDL Number: MFCD10566052
Melting Point: Boiling Point: 512.1℃ at 760 mmHg
Density: 1.46g/ml Storage Condition: Room temperature, dry, sealed
Product Description: Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted indole, makes it valuable for constructing complex heterocyclic compounds. It is often employed in the design of potential drug candidates targeting neurological disorders, such as schizophrenia and depression, due to its ability to interact with specific receptors in the brain. Additionally, its spirocyclic framework is utilized in medicinal chemistry to enhance the stability and bioavailability of therapeutic agents. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the exploration of novel chemical spaces for drug discovery.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.500 10-20 days ฿4,320.00
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1.000 10-20 days ฿6,894.00
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5.000 10-20 days ฿26,460.00
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1'-Boc-5-Bromo-1,2-dihydro-2-oxo-spiro[3H-indole-3,4'-piperidine]
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted indole, makes it valuable for constructing complex heterocyclic compounds. It is often employed in the design of potential drug candidates targeting neurological disorders, such as schizophrenia and depression, due to its ability to interact with specific receptors in the brain. Additionally, its spirocyclic framework is utilized in medicinal chemistry to enhance the stability and bioavailability of therapeutic agents. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the exploration of novel chemical spaces for drug discovery.
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