N-tert-butoxycarbonyl-8-azabicyclo [3.2.1] octane-3-carboxylic acid

95%

  • Product Code: 51656
  CAS:    1159826-74-0
Molecular Weight: 255.31 g./mol Molecular Formula: C₁₃H₂₁NO₄
EC Number: MDL Number: MFCD12068415
Melting Point: Boiling Point: 386.0±35.0 °C at 760 mmHg
Density: 1.196±0.06 g/cm3 Storage Condition: room temperature
Product Description: This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, including potential drugs targeting the central nervous system. Its bicyclic structure makes it valuable for creating rigid frameworks that can enhance the binding affinity of drug candidates to specific biological targets. Additionally, it is often employed in peptide synthesis, where the N-tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step processes. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve high enantiomeric purity in final products.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days Ft37,720.15
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1.000 10-20 days Ft93,282.23
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5.000 10-20 days Ft323,481.82
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N-tert-butoxycarbonyl-8-azabicyclo [3.2.1] octane-3-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, including potential drugs targeting the central nervous system. Its bicyclic structure makes it valuable for creating rigid frameworks that can enhance the binding affinity of drug candidates to specific biological targets. Additionally, it is often employed in peptide synthesis, where the N-tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step processes. Its application extends to the production of chiral compounds, where its stereochemistry is leveraged to achieve high enantiomeric purity in final products.
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