1-((2R,4S,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

97%

Reagent Code: #39071
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CAS Number 40733-27-5

science Other reagents with same CAS 40733-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.49 g/mol
Formula C₁₆H₂₈N₂O₅Si
badge Registry Numbers
MDL Number MFCD01631040
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a building block in the creation of modified nucleosides, enhancing their stability and bioavailability. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for the hydroxyl function, enabling selective reactions during the synthesis process. This chemical is particularly valuable in the production of antiviral agents targeting diseases such as HIV, hepatitis, and herpes, where modified nucleosides inhibit viral replication. Its application extends to research in biochemistry and molecular biology, where it aids in studying nucleic acid interactions and developing therapeutic molecules.

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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 100mg
10-20 days ฿3,380.00
inventory 250mg
10-20 days ฿4,310.00

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1-((2R,4S,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
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This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a building block in the creation of modified nucleosides, enhancing their stability and bioavailability. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for the hydroxyl function, enabling selective reactions during the synthesis process. This chemical is particularly valuable in the production of antiviral

This compound is primarily used in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a building block in the creation of modified nucleosides, enhancing their stability and bioavailability. The tert-butyldimethylsilyl (TBDMS) group serves as a protecting group for the hydroxyl function, enabling selective reactions during the synthesis process. This chemical is particularly valuable in the production of antiviral agents targeting diseases such as HIV, hepatitis, and herpes, where modified nucleosides inhibit viral replication. Its application extends to research in biochemistry and molecular biology, where it aids in studying nucleic acid interactions and developing therapeutic molecules.

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