(2R,3S,4R,5R)-5-(((Allyloxy)carbonyl)amino)-2-hydroxy-6-oxohexane-1,3,4-triyl triacetate

95%

Reagent Code: #228754
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CAS Number 1374760-23-2

science Other reagents with same CAS 1374760-23-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 389.35 g/mol
Formula C₁₆H₂₃NO₁₀
thermostat Physical Properties
Boiling Point 542.3±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.269±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of antiviral and antibiotic agents, particularly in the preparation of nucleoside analogs. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. Commonly employed in pharmaceutical research for prodrug development, where the allyl carbamate group acts as a cleavable protecting group under mild conditions. Also utilized in the production of glycosyl donors for oligosaccharide assembly due to its stereochemistry and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 500mg
10-20 days ฿6,000.00
inventory 1g
10-20 days ฿9,600.00

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(2R,3S,4R,5R)-5-(((Allyloxy)carbonyl)amino)-2-hydroxy-6-oxohexane-1,3,4-triyl triacetate
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Used as an intermediate in the synthesis of antiviral and antibiotic agents, particularly in the preparation of nucleoside analogs. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. Commonly employed in pharmaceutical research for prodrug development, where the allyl carbamate group acts as a cleavable protecting group under mild conditions. Also utilized in the production of glycosyl donors for oligosaccharide assembly due to its stereochemistry and funct

Used as an intermediate in the synthesis of antiviral and antibiotic agents, particularly in the preparation of nucleoside analogs. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. Commonly employed in pharmaceutical research for prodrug development, where the allyl carbamate group acts as a cleavable protecting group under mild conditions. Also utilized in the production of glycosyl donors for oligosaccharide assembly due to its stereochemistry and functional group compatibility.

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