6-O-(Triisopropylsilyl)-D-glucal

≥95%

Reagent Code: #103757
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CAS Number 137915-37-8

science Other reagents with same CAS 137915-37-8

blur_circular Chemical Specifications

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Weight 302.49 g/mol
Formula C₁₅H₃₀O₄Si
inventory_2 Storage & Handling
Storage room temperature

description Product Description

6-O-(Triisopropylsilyl)-D-glucal is primarily used in organic synthesis as a protected form of D-glucal. It serves as a key intermediate in the preparation of complex carbohydrates and glycoconjugates. The triisopropylsilyl (TIPS) group acts as a protecting group for the hydroxyl moiety, allowing selective modifications to other parts of the molecule without affecting the protected site. This compound is particularly valuable in the synthesis of glycosides, oligosaccharides, and other biologically active molecules. Its application extends to the development of pharmaceuticals, where it aids in the creation of sugar-based drugs and therapeutic agents. Additionally, it is utilized in research to study glycosylation reactions and carbohydrate chemistry, contributing to advancements in medicinal chemistry and biochemistry.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿891.00

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6-O-(Triisopropylsilyl)-D-glucal
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6-O-(Triisopropylsilyl)-D-glucal is primarily used in organic synthesis as a protected form of D-glucal. It serves as a key intermediate in the preparation of complex carbohydrates and glycoconjugates. The triisopropylsilyl (TIPS) group acts as a protecting group for the hydroxyl moiety, allowing selective modifications to other parts of the molecule without affecting the protected site. This compound is particularly valuable in the synthesis of glycosides, oligosaccharides, and other biologically active molecules. Its application extends to the development of pharmaceuticals, where it aids in the creation of sugar-based drugs and therapeutic agents. Additionally, it is utilized in research to study glycosylation reactions and carbohydrate chemistry, contributing to advancements in medicinal chemistry and biochemistry.
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