2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl Fluoride

≥95%

Reagent Code: #103662
fingerprint
CAS Number 89025-46-7

science Other reagents with same CAS 89025-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.65 g/mol
Formula C₃₄H₃₅FO₅
badge Registry Numbers
MDL Number MFCD03701104
thermostat Physical Properties
Melting Point 67-71°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a glycosyl donor for the formation of glycosidic bonds, particularly in carbohydrate chemistry. It is valuable for constructing complex oligosaccharides and glycoconjugates. The benzyl groups protect the hydroxyl functionalities, allowing selective reactions. It is also employed in enzymatic and chemical glycosylation studies to understand and mimic biological processes. Its stability and reactivity make it a key reagent in the development of pharmaceuticals, especially in the synthesis of glycosylated drugs and natural products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,241.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl Fluoride
No image available

Used in organic synthesis as a glycosyl donor for the formation of glycosidic bonds, particularly in carbohydrate chemistry. It is valuable for constructing complex oligosaccharides and glycoconjugates. The benzyl groups protect the hydroxyl functionalities, allowing selective reactions. It is also employed in enzymatic and chemical glycosylation studies to understand and mimic biological processes. Its stability and reactivity make it a key reagent in the development of pharmaceuticals, especially in th

Used in organic synthesis as a glycosyl donor for the formation of glycosidic bonds, particularly in carbohydrate chemistry. It is valuable for constructing complex oligosaccharides and glycoconjugates. The benzyl groups protect the hydroxyl functionalities, allowing selective reactions. It is also employed in enzymatic and chemical glycosylation studies to understand and mimic biological processes. Its stability and reactivity make it a key reagent in the development of pharmaceuticals, especially in the synthesis of glycosylated drugs and natural products.

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...