(R)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate

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Reagent Code: #230984
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CAS Number 1187929-33-4

science Other reagents with same CAS 1187929-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD06739119
thermostat Physical Properties
Boiling Point 311 °C
inventory_2 Storage & Handling
Density 1.078 g/cm3
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and morpholine ring make it valuable in medicinal chemistry for constructing complex molecules, especially in central nervous system (CNS) agents and kinase inhibitors. Commonly employed in asymmetric synthesis and catalysis due to the stability of the tert-butyl carbamate (Boc) group, allowing selective reactions at other functional sites. Also utilized in the preparation of peptidomimetics and bioactive compounds where stereochemistry plays a critical role in biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,300.00
inventory 100mg
10-20 days ฿3,960.00
inventory 250mg
10-20 days ฿9,210.00
inventory 500mg
10-20 days ฿18,420.00
inventory 1g
10-20 days ฿22,350.00

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(R)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and morpholine ring make it valuable in medicinal chemistry for constructing complex molecules, especially in central nervous system (CNS) agents and kinase inhibitors. Commonly employed in asymmetric synthesis and catalysis due to the stability of the tert-butyl carbamate (Boc) group, allowing

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and morpholine ring make it valuable in medicinal chemistry for constructing complex molecules, especially in central nervous system (CNS) agents and kinase inhibitors. Commonly employed in asymmetric synthesis and catalysis due to the stability of the tert-butyl carbamate (Boc) group, allowing selective reactions at other functional sites. Also utilized in the preparation of peptidomimetics and bioactive compounds where stereochemistry plays a critical role in biological activity.

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