tert-Butyl2-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

95%

  • Product Code: 75946
  CAS:    1707713-85-6
Molecular Weight: 347.38 g./mol Molecular Formula: C₁₈H₂₂FN₃O₃
EC Number: MDL Number: MFCD26097203
Melting Point: Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel therapeutic agents. Its structural features make it a valuable intermediate in the creation of compounds targeting central nervous system (CNS) disorders. Researchers leverage its unique spirocyclic framework to design molecules with potential activity against neurological conditions such as anxiety, depression, and neurodegenerative diseases. Additionally, its incorporation into drug candidates is explored for its ability to enhance pharmacokinetic properties, including stability and bioavailability. The compound's fluorophenyl group also contributes to its interaction with biological targets, making it a key component in the development of selective and potent inhibitors for specific enzymes or receptors. Overall, it plays a significant role in advancing medicinal chemistry and drug discovery efforts.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿118,090.00
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tert-Butyl2-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate
This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel therapeutic agents. Its structural features make it a valuable intermediate in the creation of compounds targeting central nervous system (CNS) disorders. Researchers leverage its unique spirocyclic framework to design molecules with potential activity against neurological conditions such as anxiety, depression, and neurodegenerative diseases. Additionally, its incorporation into drug candidates is explored for its ability to enhance pharmacokinetic properties, including stability and bioavailability. The compound's fluorophenyl group also contributes to its interaction with biological targets, making it a key component in the development of selective and potent inhibitors for specific enzymes or receptors. Overall, it plays a significant role in advancing medicinal chemistry and drug discovery efforts.
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