(R)-6-(Benzyloxy)-8-(oxiran-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one

97%

Reagent Code: #229306
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CAS Number 869478-12-6

science Other reagents with same CAS 869478-12-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.31 g/mol
Formula C₁₇H₁₅NO₄
badge Registry Numbers
MDL Number MFCD30729959
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the preparation of protease inhibitors and kinase inhibitors. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of diverse side chains. The benzyl-protected hydroxyl group can be deprotected and further modified to tune molecular properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid scaffold and stereochemical purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,930.00
inventory 250mg
10-20 days ฿8,380.00
inventory 1g
10-20 days ฿22,620.00
(R)-6-(Benzyloxy)-8-(oxiran-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one
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Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the preparation of protease inhibitors and kinase inhibitors. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of diverse side chains. The benzyl-protected hydroxyl group can be deprotected and further modified to tune molecular properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid scaffold

Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the preparation of protease inhibitors and kinase inhibitors. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of diverse side chains. The benzyl-protected hydroxyl group can be deprotected and further modified to tune molecular properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid scaffold and stereochemical purity.

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