2-Acetylamino-3,4,6-tri-O-acetyl-1-O-(N-Cbz-6-aminopropyl)-2-deoxy-β-D-galactopyranose

≥98%

Reagent Code: #138212
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CAS Number 143918-33-6

science Other reagents with same CAS 143918-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.54 g/mol
Formula C₂₅H₃₄N₂O₁₁
badge Registry Numbers
MDL Number MFCD34596681
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a glycosylation donor in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the preparation of biologically relevant glycolipids and glycoproteins. The presence of the Cbz-protected aminopropyl linker allows for further conjugation to carrier proteins or solid supports, making it valuable in vaccine development and immunological studies. The acetyl groups act as temporary protecting groups that can be selectively removed to enable sequential sugar coupling. Its β-configuration ensures stereocontrolled formation of glycosidic bonds, which is critical for mimicking natural carbohydrate structures in medicinal chemistry and biochemical research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿630.00
inventory 1g
10-20 days ฿1,650.00

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2-Acetylamino-3,4,6-tri-O-acetyl-1-O-(N-Cbz-6-aminopropyl)-2-deoxy-β-D-galactopyranose
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Used as a glycosylation donor in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the preparation of biologically relevant glycolipids and glycoproteins. The presence of the Cbz-protected aminopropyl linker allows for further conjugation to carrier proteins or solid supports, making it valuable in vaccine development and immunological studies. The acetyl groups act as temporary protecting groups that can be selectively removed to enable sequential sugar coupling. Its β-confi

Used as a glycosylation donor in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the preparation of biologically relevant glycolipids and glycoproteins. The presence of the Cbz-protected aminopropyl linker allows for further conjugation to carrier proteins or solid supports, making it valuable in vaccine development and immunological studies. The acetyl groups act as temporary protecting groups that can be selectively removed to enable sequential sugar coupling. Its β-configuration ensures stereocontrolled formation of glycosidic bonds, which is critical for mimicking natural carbohydrate structures in medicinal chemistry and biochemical research.

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