(2R,3R,4R)-2,3,5-Tris(benzyloxy)-4-hydroxypentanal

95%

Reagent Code: #103600
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CAS Number 54623-25-5

science Other reagents with same CAS 54623-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 420.50 g/mol
Formula C₂₆H₂₈O₅
badge Registry Numbers
MDL Number MFCD03425640
thermostat Physical Properties
Boiling Point 591.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20℃, inert gas storage

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure, featuring multiple benzyl-protected hydroxyl groups, makes it a valuable intermediate in the synthesis of oligosaccharides and other biologically active molecules. It is often employed in the construction of glycosidic linkages, where its hydroxyl groups can be selectively deprotected and functionalized. Additionally, it serves as a chiral building block in the synthesis of natural products and pharmaceuticals, enabling the creation of stereochemically defined structures. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing glycan-based therapeutics.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
Melting Point 48.0-55.0
Optical Rotation (C=4 in DCM) 59.0-67.0°C
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿963.00
inventory 100mg
10-20 days ฿297.00
inventory 250mg
10-20 days ฿360.00

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(2R,3R,4R)-2,3,5-Tris(benzyloxy)-4-hydroxypentanal
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This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure, featuring multiple benzyl-protected hydroxyl groups, makes it a valuable intermediate in the synthesis of oligosaccharides and other biologically active molecules. It is often employed in the construction of glycosidic linkages, where its hydroxyl groups can be selectively deprotected and functionalized. Additionally, it serves as a chiral building block i

This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure, featuring multiple benzyl-protected hydroxyl groups, makes it a valuable intermediate in the synthesis of oligosaccharides and other biologically active molecules. It is often employed in the construction of glycosidic linkages, where its hydroxyl groups can be selectively deprotected and functionalized. Additionally, it serves as a chiral building block in the synthesis of natural products and pharmaceuticals, enabling the creation of stereochemically defined structures. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing glycan-based therapeutics.

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