(3R,4R,5S,6R)-6-(Acetoxymethyl)-3-benzamidotetrahydro-2H-pyran-2,4,5-triyl triacetate

95%

Reagent Code: #229467
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CAS Number 14086-92-1

science Other reagents with same CAS 14086-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 451.42 g/mol
Formula C₂₁H₂₅NO₁₀
thermostat Physical Properties
Boiling Point 600.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of antibiotics, particularly in the production of cephalosporin and penicillin derivatives. Its stereochemistry allows for selective reactions in complex drug manufacturing processes. Commonly employed in pharmaceutical research to develop beta-lactamase inhibitors and other bioactive molecules. Also utilized in enzymatic studies due to its structural similarity to sugar derivatives, making it valuable in probing glycosidase activity or designing glycomimetic drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,670.00
inventory 250mg
10-20 days ฿4,540.00
inventory 1g
10-20 days ฿12,220.00

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(3R,4R,5S,6R)-6-(Acetoxymethyl)-3-benzamidotetrahydro-2H-pyran-2,4,5-triyl triacetate
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Used primarily as an intermediate in the synthesis of antibiotics, particularly in the production of cephalosporin and penicillin derivatives. Its stereochemistry allows for selective reactions in complex drug manufacturing processes. Commonly employed in pharmaceutical research to develop beta-lactamase inhibitors and other bioactive molecules. Also utilized in enzymatic studies due to its structural similarity to sugar derivatives, making it valuable in probing glycosidase activity or designing glycomi

Used primarily as an intermediate in the synthesis of antibiotics, particularly in the production of cephalosporin and penicillin derivatives. Its stereochemistry allows for selective reactions in complex drug manufacturing processes. Commonly employed in pharmaceutical research to develop beta-lactamase inhibitors and other bioactive molecules. Also utilized in enzymatic studies due to its structural similarity to sugar derivatives, making it valuable in probing glycosidase activity or designing glycomimetic drugs.

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