(S)-N-Boc-2-Hydroxymethylmorpholine

97%

Reagent Code: #234800
label
Alias N-tert-butoxycarbonyl-(S)-3-morpholine methanol; N-tert-butoxycarbonyl-(S)-2-morpholine methanol; (S)-2-hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester; (S)-N-BOC-2-hydroxymethylmorpholine; (S)-N-BOC-2-morpholine methanol; N-BOC-(S)-2-morpholine methanol; BOC-(S)-2-morpholine methanol; (S)-N-BOC-2-hydroxymethylmorpholine
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CAS Number 135065-76-8

science Other reagents with same CAS 135065-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
thermostat Physical Properties
Melting Point 60-62 °C
Boiling Point 321 °C
inventory_2 Storage & Handling
Density 1.118
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its free hydroxyl and Boc-protected amine functionalities make it valuable in selective reactions such as peptide coupling and asymmetric synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in protease inhibitors and central nervous system agents. The Boc-protected group allows for selective deprotection under mild conditions, enabling stepwise assembly of multi-functional molecules.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,350.00
inventory 25g
10-20 days ฿3,280.00
inventory 100g
10-20 days ฿11,430.00
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(S)-N-Boc-2-Hydroxymethylmorpholine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its free hydroxyl and Boc-protected amine functionalities make it valuable in selective reactions such as peptide coupling and asymmetric synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in protease inhibitors and central nervous system agents. The Boc-protected group allows for selective deprotection und
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its free hydroxyl and Boc-protected amine functionalities make it valuable in selective reactions such as peptide coupling and asymmetric synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in protease inhibitors and central nervous system agents. The Boc-protected group allows for selective deprotection under mild conditions, enabling stepwise assembly of multi-functional molecules.
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