Racemic-(3aR,4R,7aS)-tert-butyl 4-(aminomethyl)hexahydro-1h-isoindole-2(3H)-carboxylate

95%

  • Product Code: 87822
  CAS:    1250993-72-6
Molecular Weight: 254.37 g./mol Molecular Formula: C₁₄H₂₆N₂O₂
EC Number: MDL Number: MFCD12198708
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, sealed, dry
Product Description: This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structural features, such as the hexahydro-1H-isoindole core and the tert-butyl carboxylate group, make it valuable for constructing molecules with specific stereochemistry and functional groups. Researchers often employ it in medicinal chemistry to explore new therapeutic agents, especially in the fields of neurology and oncology, where precise molecular configurations are critical for biological activity. Additionally, it is used in the development of chiral compounds, aiding in the study of enantioselective reactions and their applications in drug design.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.001 10-20 days €117.06
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0.005 10-20 days €199.92
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Racemic-(3aR,4R,7aS)-tert-butyl 4-(aminomethyl)hexahydro-1h-isoindole-2(3H)-carboxylate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structural features, such as the hexahydro-1H-isoindole core and the tert-butyl carboxylate group, make it valuable for constructing molecules with specific stereochemistry and functional groups. Researchers often employ it in medicinal chemistry to explore new therapeutic agents, especially in the fields of neurology and oncology, where precise molecular configurations are critical for biological activity. Additionally, it is used in the development of chiral compounds, aiding in the study of enantioselective reactions and their applications in drug design.
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