4-Methoxyphenyl 2-O-Benzoyl-3,6-di-O-benzyl-β-D-glucopyranoside

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Reagent Code: #103726
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CAS Number 1393898-89-9

science Other reagents with same CAS 1393898-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 570.64 g/mol
Formula C₃₄H₃₄O₈
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a protected glycoside intermediate. Its structure, featuring benzyl and benzoyl protecting groups, makes it a valuable precursor for the selective deprotection and further functionalization of sugar molecules. It is often employed in the synthesis of complex oligosaccharides and glycoconjugates, which are crucial in biological and pharmaceutical research. Additionally, it serves as a key building block in the development of glycosidase inhibitors and other carbohydrate-based therapeutics. Its stability and reactivity under controlled conditions make it a preferred choice for advanced glycosylation reactions in the study of glycobiology.

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inventory 1mg
10-20 days ฿9,500.00

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4-Methoxyphenyl 2-O-Benzoyl-3,6-di-O-benzyl-β-D-glucopyranoside
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This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a protected glycoside intermediate. Its structure, featuring benzyl and benzoyl protecting groups, makes it a valuable precursor for the selective deprotection and further functionalization of sugar molecules. It is often employed in the synthesis of complex oligosaccharides and glycoconjugates, which are crucial in biological and pharmaceutical research. Additionally, it serves as a key building block in the developme

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a protected glycoside intermediate. Its structure, featuring benzyl and benzoyl protecting groups, makes it a valuable precursor for the selective deprotection and further functionalization of sugar molecules. It is often employed in the synthesis of complex oligosaccharides and glycoconjugates, which are crucial in biological and pharmaceutical research. Additionally, it serves as a key building block in the development of glycosidase inhibitors and other carbohydrate-based therapeutics. Its stability and reactivity under controlled conditions make it a preferred choice for advanced glycosylation reactions in the study of glycobiology.

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