6-Oxaspiro[2.5]octan-1-amine hydrochloride

95%

  • Product Code: 75665
  CAS:    1779133-13-9
Molecular Weight: 164 g./mol Molecular Formula: C₇H₁₄ClNO
EC Number: MDL Number: MFCD26097093
Melting Point: Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This compound is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex chemical structures. Its unique spirocyclic and oxa-containing framework makes it particularly useful in the synthesis of pharmaceuticals, especially in the creation of novel drug candidates targeting neurological disorders. The presence of the amine group allows for further functionalization, enabling the attachment of various pharmacophores to enhance biological activity. Additionally, it is employed in the preparation of specialized polymers and materials, where its structural features contribute to the desired physical and chemical properties. Researchers also explore its potential in agrochemical applications, leveraging its reactivity to develop new pesticides or herbicides.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿140,360.00
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-
5.000 10-20 days ฿459,800.00
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6-Oxaspiro[2.5]octan-1-amine hydrochloride
This compound is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex chemical structures. Its unique spirocyclic and oxa-containing framework makes it particularly useful in the synthesis of pharmaceuticals, especially in the creation of novel drug candidates targeting neurological disorders. The presence of the amine group allows for further functionalization, enabling the attachment of various pharmacophores to enhance biological activity. Additionally, it is employed in the preparation of specialized polymers and materials, where its structural features contribute to the desired physical and chemical properties. Researchers also explore its potential in agrochemical applications, leveraging its reactivity to develop new pesticides or herbicides.
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