4-Boc-2-(bromomethyl)morpholine

97%

Reagent Code: #146584
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CAS Number 765914-78-1

science Other reagents with same CAS 765914-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.16 g/mol
Formula C₁₀H₁₈BrNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The Boc-protected morpholine ring provides stability and solubility, while the bromomethyl group allows for further functionalization through nucleophilic substitution reactions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in drug discovery programs targeting oncology and central nervous system disorders. Its reactivity and structural features make it valuable for solid-phase synthesis and parallel chemistry approaches.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿880.00
inventory 100mg
10-20 days ฿1,670.00
inventory 250mg
10-20 days ฿3,310.00
inventory 1g
10-20 days ฿9,490.00
inventory 5g
10-20 days ฿42,860.00
4-Boc-2-(bromomethyl)morpholine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The Boc-protected morpholine ring provides stability and solubility, while the bromomethyl group allows for further functionalization through nucleophilic substitution reactions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in drug discovery programs targeting oncology and central nervou

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The Boc-protected morpholine ring provides stability and solubility, while the bromomethyl group allows for further functionalization through nucleophilic substitution reactions. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems, especially in drug discovery programs targeting oncology and central nervous system disorders. Its reactivity and structural features make it valuable for solid-phase synthesis and parallel chemistry approaches.

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