2,3:4,5-Di-O-isopropylidene-1-O-p-toluenesulfonyl-β-D-fructopyranose

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Reagent Code: #103672
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CAS Number 78574-35-3

science Other reagents with same CAS 78574-35-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.47 g/mol
Formula C₁₉H₂₆O₈S
badge Registry Numbers
MDL Number MFCD21496270
thermostat Physical Properties
Melting Point 83°C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis as a protected form of fructose. It serves as an intermediate in the preparation of complex carbohydrates and glycoconjugates. The isopropylidene groups protect the hydroxyl functionalities, while the p-toluenesulfonyl group acts as a leaving group, facilitating further chemical modifications. It is particularly valuable in the synthesis of nucleosides, glycosides, and other biologically active molecules. Its stability and reactivity make it a useful building block in carbohydrate chemistry, enabling precise control over stereochemistry and functional group transformations.

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inventory 1g
10-20 days ฿7,440.00

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2,3:4,5-Di-O-isopropylidene-1-O-p-toluenesulfonyl-β-D-fructopyranose
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This chemical is primarily used in organic synthesis as a protected form of fructose. It serves as an intermediate in the preparation of complex carbohydrates and glycoconjugates. The isopropylidene groups protect the hydroxyl functionalities, while the p-toluenesulfonyl group acts as a leaving group, facilitating further chemical modifications. It is particularly valuable in the synthesis of nucleosides, glycosides, and other biologically active molecules. Its stability and reactivity make it a useful b

This chemical is primarily used in organic synthesis as a protected form of fructose. It serves as an intermediate in the preparation of complex carbohydrates and glycoconjugates. The isopropylidene groups protect the hydroxyl functionalities, while the p-toluenesulfonyl group acts as a leaving group, facilitating further chemical modifications. It is particularly valuable in the synthesis of nucleosides, glycosides, and other biologically active molecules. Its stability and reactivity make it a useful building block in carbohydrate chemistry, enabling precise control over stereochemistry and functional group transformations.

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