benzyl (3R)-2-amino-3-methylpiperidine-1-carboxylate

95%

Reagent Code: #230885
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CAS Number 1933774-36-7

science Other reagents with same CAS 1933774-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.32 g/mol
Formula C₁₄H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD29924226
thermostat Physical Properties
Boiling Point 373.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.111±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and defined stereochemistry make it valuable in constructing complex molecules for drug discovery, especially in central nervous system agents and enzyme inhibitors. Commonly employed in peptide mimetics and medicinal chemistry routes where a constrained piperidine scaffold is needed. The benzyl carbamate group allows for easy deprotection under mild conditions, enabling further functionalization in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,350.00
inventory 250mg
10-20 days ฿30,650.00
inventory 1g
10-20 days ฿61,280.00

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benzyl (3R)-2-amino-3-methylpiperidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and defined stereochemistry make it valuable in constructing complex molecules for drug discovery, especially in central nervous system agents and enzyme inhibitors. Commonly employed in peptide mimetics and medicinal chemistry routes where a constrained piperidine scaffold is needed. The benzyl carbamate

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and defined stereochemistry make it valuable in constructing complex molecules for drug discovery, especially in central nervous system agents and enzyme inhibitors. Commonly employed in peptide mimetics and medicinal chemistry routes where a constrained piperidine scaffold is needed. The benzyl carbamate group allows for easy deprotection under mild conditions, enabling further functionalization in multi-step syntheses.

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