1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose

98%

Reagent Code: #103634
fingerprint
CAS Number 10548-46-6

science Other reagents with same CAS 10548-46-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.52 g/mol
Formula C₂₇H₂₈O₅
badge Registry Numbers
MDL Number MFCD02683260
thermostat Physical Properties
Melting Point 90°C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are essential in biochemical research and pharmaceutical development. Its benzyl-protected groups allow for selective deprotection, enabling precise control over the glycosylation process. This makes it valuable in the study of carbohydrate-protein interactions and the development of carbohydrate-based drugs, such as vaccines and antimicrobial agents. Additionally, it is utilized in the production of chiral building blocks for organic synthesis, contributing to the creation of enantiomerically pure compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,440.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose
No image available

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are essential in biochemical research and pharmaceutical development. Its benzyl-protected groups allow for selective deprotection, enabling precise control over the glycosylation process. This makes it valuable in the study of carbohydrate-protein interactions and the development of carbohydrate-based drugs, such as va

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are essential in biochemical research and pharmaceutical development. Its benzyl-protected groups allow for selective deprotection, enabling precise control over the glycosylation process. This makes it valuable in the study of carbohydrate-protein interactions and the development of carbohydrate-based drugs, such as vaccines and antimicrobial agents. Additionally, it is utilized in the production of chiral building blocks for organic synthesis, contributing to the creation of enantiomerically pure compounds.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...