Phenyl 3-O-Allyl-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside

≥98%

Reagent Code: #104000
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CAS Number 1017587-57-3

science Other reagents with same CAS 1017587-57-3

blur_circular Chemical Specifications

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Weight 582.76 g/mol
Formula C₃₆H₃₈O₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in carbohydrate chemistry for synthesizing complex oligosaccharides and glycoconjugates, it serves as a key intermediate. The compound is particularly valuable in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in a controlled manner. Its benzyl and allyl protecting groups allow selective deprotection, enabling precise modifications during synthesis. This chemical is instrumental in developing glycopeptides, glycolipids, and other biologically active molecules, contributing to research in glycobiology and drug development. Its application extends to the study of carbohydrate-protein interactions, aiding in the design of therapeutics and diagnostics.

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inventory 250mg
10-20 days ฿3,780.00

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Phenyl 3-O-Allyl-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
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Used in carbohydrate chemistry for synthesizing complex oligosaccharides and glycoconjugates, it serves as a key intermediate. The compound is particularly valuable in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in a controlled manner. Its benzyl and allyl protecting groups allow selective deprotection, enabling precise modifications during synthesis. This chemical is instrumental in developing glycopeptides, glycolipids, and other biologically active molecul

Used in carbohydrate chemistry for synthesizing complex oligosaccharides and glycoconjugates, it serves as a key intermediate. The compound is particularly valuable in the preparation of glycosyl donors, which are essential for constructing glycosidic bonds in a controlled manner. Its benzyl and allyl protecting groups allow selective deprotection, enabling precise modifications during synthesis. This chemical is instrumental in developing glycopeptides, glycolipids, and other biologically active molecules, contributing to research in glycobiology and drug development. Its application extends to the study of carbohydrate-protein interactions, aiding in the design of therapeutics and diagnostics.

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