(8-Benzyl-1,4-dioxa-8-aza-spiro[4.5]dec-6-yl)-methanol

95%

  • Product Code: 75736
  CAS:    64996-15-2
Molecular Weight: 263.33 g./mol Molecular Formula: C₁₅H₂₁NO₃
EC Number: MDL Number: MFCD00183312
Melting Point: Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex chemical structures. Its unique spirocyclic framework makes it valuable in the development of pharmaceuticals, particularly in the design of drugs targeting the central nervous system. The presence of the benzyl group and the dioxa-aza ring system allows for versatile reactivity, enabling modifications that can lead to compounds with potential therapeutic properties. Additionally, it may be employed in the synthesis of agrochemicals, where its structural features can contribute to the creation of active ingredients with specific biological activities. Its role as a building block in medicinal chemistry underscores its importance in the discovery and optimization of new drug candidates.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿44,830.00
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-
5.000 10-20 days ฿134,710.00
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(8-Benzyl-1,4-dioxa-8-aza-spiro[4.5]dec-6-yl)-methanol
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex chemical structures. Its unique spirocyclic framework makes it valuable in the development of pharmaceuticals, particularly in the design of drugs targeting the central nervous system. The presence of the benzyl group and the dioxa-aza ring system allows for versatile reactivity, enabling modifications that can lead to compounds with potential therapeutic properties. Additionally, it may be employed in the synthesis of agrochemicals, where its structural features can contribute to the creation of active ingredients with specific biological activities. Its role as a building block in medicinal chemistry underscores its importance in the discovery and optimization of new drug candidates.
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