6-(p-Toluenesulfonyl)-2-oxa-6-azaspiro[3.3]heptane

95%

  • Product Code: 67860
  CAS:    13573-28-9
Molecular Weight: 253.32 g./mol Molecular Formula: C₁₂H₁₅NO₃S
EC Number: MDL Number: MFCD13180735
Melting Point: 142-146℃ Boiling Point: 411℃ at 760 mmHg
Density: 1.37g/ml Storage Condition: 2-8°C, dry, sealed
Product Description: 6-(p-Toluenesulfonyl)-2-oxa-6-azaspiro[3.3]heptane is primarily used in organic synthesis as a versatile building block for constructing complex molecular structures. Its spirocyclic framework and functional groups make it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential therapeutic properties. Additionally, it is utilized in the design of novel materials and catalysts, where its unique structure can impart specific reactivity or stability. Its tosyl group also facilitates further chemical modifications, making it a useful reagent in multi-step synthetic processes.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿560.00
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1.000 10-20 days ฿1,880.00
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5.000 10-20 days ฿8,790.00
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25.000 10-20 days ฿36,480.00
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6-(p-Toluenesulfonyl)-2-oxa-6-azaspiro[3.3]heptane
6-(p-Toluenesulfonyl)-2-oxa-6-azaspiro[3.3]heptane is primarily used in organic synthesis as a versatile building block for constructing complex molecular structures. Its spirocyclic framework and functional groups make it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential therapeutic properties. Additionally, it is utilized in the design of novel materials and catalysts, where its unique structure can impart specific reactivity or stability. Its tosyl group also facilitates further chemical modifications, making it a useful reagent in multi-step synthetic processes.
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