1-Naphthyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside

≥98%

Reagent Code: #214626
fingerprint
CAS Number 121356-12-5

science Other reagents with same CAS 121356-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 473.47 g/mol
Formula C₂₄H₂₇NO₉
badge Registry Numbers
MDL Number MFCD08703862
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a glycosyl donor in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its protected acetyl groups allow selective deprotection and further chain elongation, making it valuable in the preparation of biologically active glycan structures. Commonly employed in enzymatic and chemical glycosylation studies to model natural glycosylation pathways. Also serves as an intermediate in the development of glycosidase inhibitors and vaccine candidates targeting bacterial polysaccharides.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿15,020.00
250mg
10-20 days ฿30,030.00
1g
10-20 days ฿90,090.00
1-Naphthyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside
No image available

Used as a glycosyl donor in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its protected acetyl groups allow selective deprotection and further chain elongation, making it valuable in the preparation of biologically active glycan structures. Commonly employed in enzymatic and chemical glycosylation studies to model natural glycosylation pathways. Also serves as an intermediate in the development of glycosidase inhibitors and vaccine candidates targe

Used as a glycosyl donor in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its protected acetyl groups allow selective deprotection and further chain elongation, making it valuable in the preparation of biologically active glycan structures. Commonly employed in enzymatic and chemical glycosylation studies to model natural glycosylation pathways. Also serves as an intermediate in the development of glycosidase inhibitors and vaccine candidates targeting bacterial polysaccharides.

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...