tert-Butyl ((3R,6R)-6-methylpiperidin-3-yl)carbamate

95%

Reagent Code: #229122
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CAS Number 1799311-98-0

science Other reagents with same CAS 1799311-98-0

blur_circular Chemical Specifications

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Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD26405706
inventory_2 Storage & Handling
Storage Room temperature

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) agents. Its chiral piperidine backbone supports structural specificity required for high target selectivity in drug candidates. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the tert-butyloxycarbonyl (Boc) protecting group, which allows for controlled amine reactivity during multi-step syntheses. Found in routes to treatments for neurological disorders and oncology-related therapies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿38,970.00

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tert-Butyl ((3R,6R)-6-methylpiperidin-3-yl)carbamate
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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) agents. Its chiral piperidine backbone supports structural specificity required for high target selectivity in drug candidates. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the tert-butyloxycarbonyl (Boc) protecting group, which allows for controlled amine reactivity during multi-step syntheses. Found in routes to tre

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its chiral piperidine backbone supports structural specificity required for high target selectivity in drug candidates. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the tert-butyloxycarbonyl (Boc) protecting group, which allows for controlled amine reactivity during multi-step syntheses. Found in routes to treatments for neurological disorders and oncology-related therapies.

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