(2S,3R,4R,5R)-5-((Benzoyloxy)methyl)-3-methyltetrahydrofuran-2,3,4-triyl tribenzoate

98%

Reagent Code: #97066
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CAS Number 15397-15-6

science Other reagents with same CAS 15397-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 580.58 g/mol
Formula C₃₄H₂₈O₉
thermostat Physical Properties
Melting Point 154-156°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a protected form of a sugar derivative. It serves as an intermediate in the preparation of complex carbohydrates and nucleosides, which are crucial in the development of pharmaceuticals and biochemical research. The benzoyl groups provide stability and protection to the reactive hydroxyl groups during chemical reactions, enabling selective modifications. It is also employed in the synthesis of glycosides and other biologically active molecules, contributing to advancements in drug discovery and the study of carbohydrate-based therapeutics.

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Test Parameter Specification
Appearance solid
Purity 98-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,062.00
inventory 250mg
10-20 days ฿342.00

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(2S,3R,4R,5R)-5-((Benzoyloxy)methyl)-3-methyltetrahydrofuran-2,3,4-triyl tribenzoate
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This chemical is primarily utilized in organic synthesis as a protected form of a sugar derivative. It serves as an intermediate in the preparation of complex carbohydrates and nucleosides, which are crucial in the development of pharmaceuticals and biochemical research. The benzoyl groups provide stability and protection to the reactive hydroxyl groups during chemical reactions, enabling selective modifications. It is also employed in the synthesis of glycosides and other biologically active molecules,

This chemical is primarily utilized in organic synthesis as a protected form of a sugar derivative. It serves as an intermediate in the preparation of complex carbohydrates and nucleosides, which are crucial in the development of pharmaceuticals and biochemical research. The benzoyl groups provide stability and protection to the reactive hydroxyl groups during chemical reactions, enabling selective modifications. It is also employed in the synthesis of glycosides and other biologically active molecules, contributing to advancements in drug discovery and the study of carbohydrate-based therapeutics.

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