2,4,6-tris(benzyloxy)-1,3,5-triazine

≥95%

Reagent Code: #239545
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CAS Number 7285-83-8

science Other reagents with same CAS 7285-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.4 g/mol
Formula C₂₄H₂₁N₃O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a versatile protecting group reagent in organic synthesis, particularly for hydroxyl groups. Its ability to selectively protect alcohols under mild conditions makes it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. It is also employed in carbohydrate chemistry where multiple hydroxyl groups require selective protection. The benzyloxy groups can be removed under hydrogenolytic conditions, allowing for deprotection without affecting other sensitive functional groups. Additionally, it serves as a building block in the preparation of triazine-based frameworks for materials science and medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,900.00
inventory 5g
10-20 days ฿11,040.00
2,4,6-tris(benzyloxy)-1,3,5-triazine
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Used as a versatile protecting group reagent in organic synthesis, particularly for hydroxyl groups. Its ability to selectively protect alcohols under mild conditions makes it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. It is also employed in carbohydrate chemistry where multiple hydroxyl groups require selective protection. The benzyloxy groups can be removed under hydrogenolytic conditions, allowing for deprotection without affecting other sensitive func

Used as a versatile protecting group reagent in organic synthesis, particularly for hydroxyl groups. Its ability to selectively protect alcohols under mild conditions makes it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. It is also employed in carbohydrate chemistry where multiple hydroxyl groups require selective protection. The benzyloxy groups can be removed under hydrogenolytic conditions, allowing for deprotection without affecting other sensitive functional groups. Additionally, it serves as a building block in the preparation of triazine-based frameworks for materials science and medicinal chemistry applications.

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