trans-3-Aminocyclobutanol hydrochloride

95%

  • Product Code: 122340
  CAS:    1205037-95-1
Molecular Weight: 123.58 g./mol Molecular Formula: C₄H₁₀ClNO
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: Trans-3-Aminocyclobutanol hydrochloride is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its unique cyclobutane structure, combined with the presence of both amino and hydroxyl groups, makes it a valuable building block for designing molecules with specific biological activities. It is often employed in the synthesis of potential drug candidates targeting neurological disorders, as the cyclobutane ring can enhance the rigidity and stability of the resulting compounds. Additionally, it serves as a precursor in the preparation of chiral ligands and catalysts used in asymmetric synthesis, enabling the production of enantiomerically pure substances. Its applications also extend to the field of medicinal chemistry, where it is explored for the development of novel therapeutic agents with improved efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿567.00
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0.250 10-20 days ฿1,476.00
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1.000 10-20 days ฿3,321.00
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5.000 10-20 days ฿15,435.00
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trans-3-Aminocyclobutanol hydrochloride
Trans-3-Aminocyclobutanol hydrochloride is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its unique cyclobutane structure, combined with the presence of both amino and hydroxyl groups, makes it a valuable building block for designing molecules with specific biological activities. It is often employed in the synthesis of potential drug candidates targeting neurological disorders, as the cyclobutane ring can enhance the rigidity and stability of the resulting compounds. Additionally, it serves as a precursor in the preparation of chiral ligands and catalysts used in asymmetric synthesis, enabling the production of enantiomerically pure substances. Its applications also extend to the field of medicinal chemistry, where it is explored for the development of novel therapeutic agents with improved efficacy and selectivity.
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