((2S,4S)-4-Acetoxy-3,4-dihydro-2H-pyran-2-yl)methyl acetate

95%

Reagent Code: #232511
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CAS Number 13036-11-8

science Other reagents with same CAS 13036-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.22 g/mol
Formula C₁₀H₁₄O₅
thermostat Physical Properties
Boiling Point 87-93 °C at 10-13 mmHg
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its stereochemistry allows for selective glycosylation reactions, making it valuable in pharmaceutical research for developing biologically active compounds. Commonly employed in the construction of modified sugar moieties found in prodrugs and therapeutic agents targeting viral replication, including HIV and hepatitis viruses. Also utilized in organic synthesis for chiral building blocks due to its stable ring structure and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,220.00
inventory 100mg
10-20 days ฿15,650.00

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((2S,4S)-4-Acetoxy-3,4-dihydro-2H-pyran-2-yl)methyl acetate
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Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its stereochemistry allows for selective glycosylation reactions, making it valuable in pharmaceutical research for developing biologically active compounds. Commonly employed in the construction of modified sugar moieties found in prodrugs and therapeutic agents targeting viral replication, including HIV and hepatitis viruses. Also utilized in organic synthesis for chiral

Used as a key intermediate in the synthesis of antiviral and antitumor agents, particularly in the preparation of nucleoside analogs. Its stereochemistry allows for selective glycosylation reactions, making it valuable in pharmaceutical research for developing biologically active compounds. Commonly employed in the construction of modified sugar moieties found in prodrugs and therapeutic agents targeting viral replication, including HIV and hepatitis viruses. Also utilized in organic synthesis for chiral building blocks due to its stable ring structure and functional group compatibility.

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