(4R,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-3-chlorodihydrofuran-2(3H)-onelactone, (2ξ)-

97%

Reagent Code: #228641
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CAS Number 1820749-52-7

science Other reagents with same CAS 1820749-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 395.08 g/mol
Formula C₁₇H₃₅ClO₄Si₂
badge Registry Numbers
MDL Number MFCD29922374
thermostat Physical Properties
Boiling Point 403.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.01±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of antiviral and antitumor agents. Its silyl-protected hydroxyl groups allow for selective reactivity and stability during multi-step organic transformations. Commonly employed in nucleoside analog synthesis, where the chloro and lactone functionalities enable further ring modifications and coupling reactions. The stereochemistry supports high enantioselectivity in downstream processes, making it valuable in asymmetric synthesis.

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inventory 1g
10-20 days ฿21,000.00

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(4R,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-3-chlorodihydrofuran-2(3H)-onelactone, (2ξ)-
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Used as a key chiral intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of antiviral and antitumor agents. Its silyl-protected hydroxyl groups allow for selective reactivity and stability during multi-step organic transformations. Commonly employed in nucleoside analog synthesis, where the chloro and lactone functionalities enable further ring modifications and coupling reactions. The stereochemistry supports high enantioselectivity in downstrea

Used as a key chiral intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of antiviral and antitumor agents. Its silyl-protected hydroxyl groups allow for selective reactivity and stability during multi-step organic transformations. Commonly employed in nucleoside analog synthesis, where the chloro and lactone functionalities enable further ring modifications and coupling reactions. The stereochemistry supports high enantioselectivity in downstream processes, making it valuable in asymmetric synthesis.

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