tert-Butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylate

≥95%

  • Product Code: 126286
  CAS:    1198408-35-3
Molecular Weight: 277.36 g./mol Molecular Formula: C15H23N3O2
EC Number: MDL Number: MFCD11111266
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, protected from light, dry and sealed
Product Description: This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a piperidine ring and an aminopyridine moiety, makes it valuable for designing compounds targeting central nervous system disorders, such as neurological and psychiatric conditions. It is often employed in the creation of potential drug candidates that interact with receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers also explore its use in developing inhibitors for specific proteins or pathways implicated in diseases like cancer or inflammation. Its role in optimizing drug-like properties, such as bioavailability and selectivity, further underscores its importance in drug discovery.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿450.00
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-
0.250 10-20 days ฿810.00
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1.000 10-20 days ฿2,440.00
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5.000 10-20 days ฿9,220.00
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-
10.000 10-20 days ฿17,860.00
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-
tert-Butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a piperidine ring and an aminopyridine moiety, makes it valuable for designing compounds targeting central nervous system disorders, such as neurological and psychiatric conditions. It is often employed in the creation of potential drug candidates that interact with receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers also explore its use in developing inhibitors for specific proteins or pathways implicated in diseases like cancer or inflammation. Its role in optimizing drug-like properties, such as bioavailability and selectivity, further underscores its importance in drug discovery.
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