tert-Butyl ((3S,5S)-5-methylpiperidin-3-yl)carbamate

98%

Reagent Code: #233538
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CAS Number 951163-61-4

science Other reagents with same CAS 951163-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD11112079
thermostat Physical Properties
Boiling Point 313 °C
inventory_2 Storage & Handling
Density 1.00 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as neurological and psychiatric disorder treatments. Its chiral piperidine backbone makes it valuable in constructing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and conformational rigidity it imparts. The tert-butyloxycarbonyl (Boc) group allows for easy protection of the amine during peptide coupling or multistep synthesis, enabling efficient derivatization. Widely utilized in the preparation of kinase inhibitors, receptor agonists, and antagonists where stereochemistry plays a critical role in efficacy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿8,000.00
inventory 500mg
10-20 days ฿12,800.00
inventory 5g
10-20 days ฿32,000.00
inventory 10g
10-20 days ฿48,000.00
inventory 1g
10-20 days ฿16,000.00

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tert-Butyl ((3S,5S)-5-methylpiperidin-3-yl)carbamate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as neurological and psychiatric disorder treatments. Its chiral piperidine backbone makes it valuable in constructing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and conformational rigidity it imparts. The tert-butyloxycarbonyl (Boc) group allows for easy protection of

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as neurological and psychiatric disorder treatments. Its chiral piperidine backbone makes it valuable in constructing bioactive molecules with high selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and conformational rigidity it imparts. The tert-butyloxycarbonyl (Boc) group allows for easy protection of the amine during peptide coupling or multistep synthesis, enabling efficient derivatization. Widely utilized in the preparation of kinase inhibitors, receptor agonists, and antagonists where stereochemistry plays a critical role in efficacy.

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