1'-(tert-Butoxycarbonyl)spiro[bicyclo[2.2.1]-heptane-7,4'-piperidine]-2-carboxylic acid

95%

  • Product Code: 74806
  CAS:    1250998-00-5
Molecular Weight: 309.41 g./mol Molecular Formula: C₁₇H₂₇NO₄
EC Number: MDL Number: MFCD12198777
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, ventilated
Product Description: This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the creation of complex molecules, often employed in the synthesis of biologically active compounds. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and protecting amine functionalities during multi-step synthetic processes. Researchers often use it in the design of drug candidates targeting neurological disorders, as its bicyclic and piperidine components are common motifs in central nervous system (CNS) drugs. Additionally, its carboxylic acid group allows for further functionalization, enabling the attachment of various pharmacophores to enhance drug efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.001 10-20 days $691.50
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1'-(tert-Butoxycarbonyl)spiro[bicyclo[2.2.1]-heptane-7,4'-piperidine]-2-carboxylic acid
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the creation of complex molecules, often employed in the synthesis of biologically active compounds. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and protecting amine functionalities during multi-step synthetic processes. Researchers often use it in the design of drug candidates targeting neurological disorders, as its bicyclic and piperidine components are common motifs in central nervous system (CNS) drugs. Additionally, its carboxylic acid group allows for further functionalization, enabling the attachment of various pharmacophores to enhance drug efficacy and selectivity.
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