Benzyl 2,3:5,6-Di-O-isopropylidene-α-D-mannofuranoside

≥97.0%

Reagent Code: #96951
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CAS Number 20689-02-5

science Other reagents with same CAS 20689-02-5

blur_circular Chemical Specifications

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Weight 350.41 g/mol
Formula C₁₉H₂₆O₆
inventory_2 Storage & Handling
Storage -20°C, sealed, dry, inert gas

description Product Description

Used primarily in organic synthesis as a protected form of mannose, this compound is valuable in carbohydrate chemistry for constructing complex glycostructures. It serves as an intermediate in the production of glycosides and glycoconjugates, which are crucial in developing pharmaceuticals, especially in the synthesis of antiviral and anticancer drugs. Additionally, it is employed in the study of enzyme mechanisms and in the preparation of chiral catalysts, aiding in asymmetric synthesis processes. Its stability under various conditions makes it a preferred choice for research and industrial applications in medicinal chemistry.

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inventory 500mg
10-20 days ฿8,811.00

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Benzyl 2,3:5,6-Di-O-isopropylidene-α-D-mannofuranoside
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Used primarily in organic synthesis as a protected form of mannose, this compound is valuable in carbohydrate chemistry for constructing complex glycostructures. It serves as an intermediate in the production of glycosides and glycoconjugates, which are crucial in developing pharmaceuticals, especially in the synthesis of antiviral and anticancer drugs. Additionally, it is employed in the study of enzyme mechanisms and in the preparation of chiral catalysts, aiding in asymmetric synthesis processes. Its

Used primarily in organic synthesis as a protected form of mannose, this compound is valuable in carbohydrate chemistry for constructing complex glycostructures. It serves as an intermediate in the production of glycosides and glycoconjugates, which are crucial in developing pharmaceuticals, especially in the synthesis of antiviral and anticancer drugs. Additionally, it is employed in the study of enzyme mechanisms and in the preparation of chiral catalysts, aiding in asymmetric synthesis processes. Its stability under various conditions makes it a preferred choice for research and industrial applications in medicinal chemistry.

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