(2R,3R,4S,5R,6R)-2-(Hydroxymethyl)-6-(3-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol

95%

Reagent Code: #230750
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CAS Number 52571-71-8

science Other reagents with same CAS 52571-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.25 g/mol
Formula C₁₂H₁₅NO₈
badge Registry Numbers
MDL Number MFCD00067358
thermostat Physical Properties
Boiling Point 573.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, inert gas storage

description Product Description

Used in pharmaceutical research as a glycoside analog for developing enzyme inhibitors, particularly targeting glycosidases involved in carbohydrate metabolism. Its modified sugar structure with a nitrophenoxy group enables use in prodrug designs and as a biochemical tool for studying glycosylation processes. Also investigated for potential antiviral and anticancer applications due to its ability to interfere with cellular glycoprotein synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,870.00
inventory 250mg
10-20 days ฿11,020.00
inventory 1g
10-20 days ฿26,440.00

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(2R,3R,4S,5R,6R)-2-(Hydroxymethyl)-6-(3-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol
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Used in pharmaceutical research as a glycoside analog for developing enzyme inhibitors, particularly targeting glycosidases involved in carbohydrate metabolism. Its modified sugar structure with a nitrophenoxy group enables use in prodrug designs and as a biochemical tool for studying glycosylation processes. Also investigated for potential antiviral and anticancer applications due to its ability to interfere with cellular glycoprotein synthesis.

Used in pharmaceutical research as a glycoside analog for developing enzyme inhibitors, particularly targeting glycosidases involved in carbohydrate metabolism. Its modified sugar structure with a nitrophenoxy group enables use in prodrug designs and as a biochemical tool for studying glycosylation processes. Also investigated for potential antiviral and anticancer applications due to its ability to interfere with cellular glycoprotein synthesis.

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