2,3,5-Tri-o-benzyl-1-o-(4-nitrobenzoyl)-D-arabinofuranose

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Reagent Code: #97074
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CAS Number 52522-49-3

science Other reagents with same CAS 52522-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 569.6 g/mol
Formula C₃₃H₃₁NO₈
badge Registry Numbers
MDL Number MFCD00038477
thermostat Physical Properties
Melting Point 86-88°C
Boiling Point 706.2°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis, this chemical serves as a key intermediate in the preparation of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its benzyl and nitrobenzoyl protecting groups allow selective deprotection, enabling precise modifications to the sugar moiety. This specificity is vital in creating structurally diverse compounds for pharmaceutical research. Additionally, it plays a role in carbohydrate chemistry, aiding in the study of glycosylation reactions and the synthesis of complex oligosaccharides. Its applications extend to the development of novel therapeutic agents and the exploration of biochemical pathways.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,390.00
inventory 250mg
10-20 days ฿620.00
inventory 1g
10-20 days ฿1,850.00

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2,3,5-Tri-o-benzyl-1-o-(4-nitrobenzoyl)-D-arabinofuranose
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Used primarily in organic synthesis, this chemical serves as a key intermediate in the preparation of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its benzyl and nitrobenzoyl protecting groups allow selective deprotection, enabling precise modifications to the sugar moiety. This specificity is vital in creating structurally diverse compounds for pharmaceutical research. Additionally, it plays a role in carbohydrate chemistry, aiding in the study of glycosylation re

Used primarily in organic synthesis, this chemical serves as a key intermediate in the preparation of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. Its benzyl and nitrobenzoyl protecting groups allow selective deprotection, enabling precise modifications to the sugar moiety. This specificity is vital in creating structurally diverse compounds for pharmaceutical research. Additionally, it plays a role in carbohydrate chemistry, aiding in the study of glycosylation reactions and the synthesis of complex oligosaccharides. Its applications extend to the development of novel therapeutic agents and the exploration of biochemical pathways.

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