tert-Butyl 4-amino-2-isopropylpiperidine-1-carboxylate

95%

Reagent Code: #151935
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CAS Number 1558365-90-4

science Other reagents with same CAS 1558365-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.36 g/mol
Formula C₁₃H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD24533667
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active agents. Its piperidine backbone with a protected amine group allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. Also utilized in the preparation of bioactive compounds requiring chiral, substituted piperidines for enhanced selectivity and potency.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,230.00
inventory 50mg
10-20 days ฿13,860.00
inventory 100mg
10-20 days ฿20,780.00
inventory 250mg
10-20 days ฿31,160.00
inventory 1g
10-20 days ฿84,370.00

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tert-Butyl 4-amino-2-isopropylpiperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active agents. Its piperidine backbone with a protected amine group allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. Also utili

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active agents. Its piperidine backbone with a protected amine group allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. Also utilized in the preparation of bioactive compounds requiring chiral, substituted piperidines for enhanced selectivity and potency.

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