3'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-2-thiomethyl benzophenone

97%

  • Product Code: 75368
  CAS:    898761-65-4
Molecular Weight: 383.51 g./mol Molecular Formula: C₂₂H₂₅NO₃S
EC Number: MDL Number: MFCD03842190
Melting Point: Boiling Point: 552.4℃ at 760 mmHg
Density: 1.25g/ml Storage Condition: Room temperature, sealed, ventilated
Product Description: This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. Its structure, featuring a benzophenone core with a thiomethyl group and a dioxa-azaspiro moiety, makes it a valuable intermediate in the development of complex molecules. It is often employed in the synthesis of potential drug candidates, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways. Additionally, its unique spirocyclic structure is explored in the design of novel materials with potential applications in organic electronics and photochemistry. Researchers also investigate its use in creating advanced ligands for catalysis, enhancing the efficiency of chemical reactions.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $2,729.08
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2.000 10-20 days $4,533.90
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3'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]-2-thiomethyl benzophenone
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. Its structure, featuring a benzophenone core with a thiomethyl group and a dioxa-azaspiro moiety, makes it a valuable intermediate in the development of complex molecules. It is often employed in the synthesis of potential drug candidates, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways. Additionally, its unique spirocyclic structure is explored in the design of novel materials with potential applications in organic electronics and photochemistry. Researchers also investigate its use in creating advanced ligands for catalysis, enhancing the efficiency of chemical reactions.
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