S-1-Boc-3-(methylamino)piperidine

97%

Reagent Code: #234229
label
Alias (S)-1-tert-butoxycarbonyl-3-(methylamino)piperidine
fingerprint
CAS Number 912368-73-1

science Other reagents with same CAS 912368-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD09752964
thermostat Physical Properties
Boiling Point 289℃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly the S-enantiomer in the development of centrally acting agents such as opioid receptor modulators. Its Boc-protected piperidine nitrogen allows for selective reactions at the 3-(methylamino) group in multi-step syntheses, making it valuable in creating structurally complex drug candidates with defined stereochemistry. Commonly employed in medicinal chemistry for building piperidine-based scaffolds found in bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,440.00
inventory 5g
10-20 days ฿13,200.00
inventory 10g
10-20 days ฿26,100.00
inventory 25g
10-20 days ฿64,500.00
S-1-Boc-3-(methylamino)piperidine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly the S-enantiomer in the development of centrally acting agents such as opioid receptor modulators. Its Boc-protected piperidine nitrogen allows for selective reactions at the 3-(methylamino) group in multi-step syntheses, making it valuable in creating structurally complex drug candidates with defined stereochemistry. Commonly employed in medicinal chemistry for building piperidine-based scaffolds found in bioactive molec

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly the S-enantiomer in the development of centrally acting agents such as opioid receptor modulators. Its Boc-protected piperidine nitrogen allows for selective reactions at the 3-(methylamino) group in multi-step syntheses, making it valuable in creating structurally complex drug candidates with defined stereochemistry. Commonly employed in medicinal chemistry for building piperidine-based scaffolds found in bioactive molecules.

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