tert-Butyl 4-(4-(aminomethyl)benzoyl)piperazine-1-carboxylate

98%

  • Product Code: 46264
  CAS:    1299397-08-2
Molecular Weight: 319.3987 g./mol Molecular Formula: C₁₇H₂₅N₃O₃
EC Number: MDL Number: MFCD33395921
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both a piperazine ring and an aminomethylbenzoyl group, makes it a versatile building block for developing molecules with potential biological activity. It is often employed in the design and preparation of drug candidates targeting neurological disorders, such as anxiety, depression, and schizophrenia, due to its ability to interact with neurotransmitter receptors. Additionally, its tert-butyl carboxylate group provides stability and ease of modification, making it valuable in organic synthesis and drug discovery processes. Researchers also explore its use in creating compounds with anti-inflammatory or antimicrobial properties, leveraging its structural framework for optimized drug efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $186.88
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tert-Butyl 4-(4-(aminomethyl)benzoyl)piperazine-1-carboxylate
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both a piperazine ring and an aminomethylbenzoyl group, makes it a versatile building block for developing molecules with potential biological activity. It is often employed in the design and preparation of drug candidates targeting neurological disorders, such as anxiety, depression, and schizophrenia, due to its ability to interact with neurotransmitter receptors. Additionally, its tert-butyl carboxylate group provides stability and ease of modification, making it valuable in organic synthesis and drug discovery processes. Researchers also explore its use in creating compounds with anti-inflammatory or antimicrobial properties, leveraging its structural framework for optimized drug efficacy and selectivity.
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