Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside

≥97%

Reagent Code: #103846
fingerprint
CAS Number 910805-49-1

science Other reagents with same CAS 910805-49-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 475.56 g/mol
Formula C₂₇H₂₅NO₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in the development of glycosidase inhibitors, which are important in the study of enzyme mechanisms and the treatment of metabolic disorders. Additionally, it is used in the synthesis of glycosyl donors, which are crucial for constructing oligosaccharides and glycoconjugates. These compounds have significant applications in drug discovery, especially in the design of antiviral, anticancer, and anti-inflammatory agents. Its unique structure allows for selective modifications, making it valuable in the production of biologically active molecules and in the advancement of glycobiology research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,109.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Phenyl N-Benzyl-2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside
No image available
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in the development of glycosidase inhibitors, which are important in the study of enzyme mechanisms and the treatment of metabolic disorders. Additionally, it is used in the synthesis of glycosyl donors, which are crucial for constructing oligosaccharides and glycoconjugates. These compounds have significant applications in drug discovery, especially in the design of antiviral, anticancer, and anti-inflammatory agents. Its unique structure allows for selective modifications, making it valuable in the production of biologically active molecules and in the advancement of glycobiology research.
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...