4-Boc-2-(aminomethyl)morpholine

≥97%

Reagent Code: #56730
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CAS Number 140645-53-0

science Other reagents with same CAS 140645-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD06410633
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

4-Boc-2-(aminomethyl)morpholine is widely used in organic synthesis, particularly as a building block for the preparation of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the compound allows for selective deprotection, enabling controlled reactions during multi-step synthesis processes. This chemical is also valuable in peptide chemistry, where it aids in the modification and stabilization of peptide structures. Additionally, it finds application in the creation of ligands and catalysts used in asymmetric synthesis, contributing to the production of enantiomerically pure compounds. Its versatility makes it a crucial component in medicinal chemistry and drug discovery research.

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Test Parameter Specification
Appearance White Crystalline
Purity (%) 97-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,241.00
inventory 1g
10-20 days ฿5,418.00

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4-Boc-2-(aminomethyl)morpholine
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4-Boc-2-(aminomethyl)morpholine is widely used in organic synthesis, particularly as a building block for the preparation of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of active pharmaceutical ingredients (APIs) and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the compound allows for selective deprotection, enabling controlled reactions during multi-step synthesis processes. This chemical is also valuable in peptide chemistry, where it aids in the modification and stabilization of peptide structures. Additionally, it finds application in the creation of ligands and catalysts used in asymmetric synthesis, contributing to the production of enantiomerically pure compounds. Its versatility makes it a crucial component in medicinal chemistry and drug discovery research.
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