benzyl 4-amino-4-methylpiperidine-1-carboxylate

98%

Reagent Code: #153797
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CAS Number 169750-59-8

science Other reagents with same CAS 169750-59-8

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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its piperidine core with a protected amine group makes it valuable in medicinal chemistry for constructing complex structures, especially in central nervous system agents and receptor modulators. The benzyl carbamate (Cbz) protecting group allows for selective deprotection under mild conditions, enabling stepwise synthesis in peptide-like or heterocyclic compounds. Also employed in the preparation of protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,660.00
inventory 250mg
10-20 days ฿2,780.00
inventory 1g
10-20 days ฿6,940.00
inventory 5g
10-20 days ฿22,720.00
inventory 10g
10-20 days ฿42,550.00

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benzyl 4-amino-4-methylpiperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its piperidine core with a protected amine group makes it valuable in medicinal chemistry for constructing complex structures, especially in central nervous system agents and receptor modulators. The benzyl carbamate (Cbz) protecting group allows for selective deprotection under mild conditions, enabling stepwise synthesis in peptide-like or heterocyclic compounds. Also employe

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its piperidine core with a protected amine group makes it valuable in medicinal chemistry for constructing complex structures, especially in central nervous system agents and receptor modulators. The benzyl carbamate (Cbz) protecting group allows for selective deprotection under mild conditions, enabling stepwise synthesis in peptide-like or heterocyclic compounds. Also employed in the preparation of protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites.

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