Benzyl 2,3,4-Tri-O-benzyl-α-D-glucopyranoside

≥98%

Reagent Code: #103980
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CAS Number 59935-49-8

science Other reagents with same CAS 59935-49-8

blur_circular Chemical Specifications

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Weight 540.652 g/mol
Formula C₃₄H₃₆O₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its benzyl-protected groups make it valuable in selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. Additionally, it is employed in the development of glycoconjugates, which are essential in drug discovery and biochemical research. Its stability and reactivity also make it suitable for use in enzymatic studies and the production of glycosidase inhibitors.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,982.00
inventory 100mg
10-20 days ฿1,287.00
inventory 500mg
10-20 days ฿4,671.00

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Benzyl 2,3,4-Tri-O-benzyl-α-D-glucopyranoside
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This chemical is primarily utilized in organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its benzyl-protected groups make it valuable in selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. Additionally, it is employed in the development of glycoconjugates, which are essential in drug discovery and biochemical research. Its stability and reactivity also make it su

This chemical is primarily utilized in organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its benzyl-protected groups make it valuable in selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. Additionally, it is employed in the development of glycoconjugates, which are essential in drug discovery and biochemical research. Its stability and reactivity also make it suitable for use in enzymatic studies and the production of glycosidase inhibitors.

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