(3As,4R,6S,6Ar)-6-(2-((Tert-Butyldimethylsilyl)Oxy)Ethoxy)-2,2-Dimethyltetrahydro-3Ah-Cyclopenta[D][1,3]Dioxol-4-Amine

98%

Reagent Code: #138938
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CAS Number 1400665-85-1

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blur_circular Chemical Specifications

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Weight 331.52 g/mol
Formula C₁₆H₃₃NO₄Si
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its protected amine and hydroxyl groups make it a valuable chiral building block for stereoselective reactions. Commonly employed in nucleoside analog synthesis, where the silyl protecting group allows for selective functionalization, and the rigid cyclopentane backbone supports proper spatial orientation in coupling reactions. Frequently utilized in antiviral and anticancer drug development due to its structural similarity to sugar moieties in nucleic acids.

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inventory 100mg
10-20 days ฿23,170.00

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(3As,4R,6S,6Ar)-6-(2-((Tert-Butyldimethylsilyl)Oxy)Ethoxy)-2,2-Dimethyltetrahydro-3Ah-Cyclopenta[D][1,3]Dioxol-4-Amine
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Used in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its protected amine and hydroxyl groups make it a valuable chiral building block for stereoselective reactions. Commonly employed in nucleoside analog synthesis, where the silyl protecting group allows for selective functionalization, and the rigid cyclopentane backbone supports proper spatial orientation in coupling reactions. Frequently utilized in antiviral and anticancer drug development due to

Used in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its protected amine and hydroxyl groups make it a valuable chiral building block for stereoselective reactions. Commonly employed in nucleoside analog synthesis, where the silyl protecting group allows for selective functionalization, and the rigid cyclopentane backbone supports proper spatial orientation in coupling reactions. Frequently utilized in antiviral and anticancer drug development due to its structural similarity to sugar moieties in nucleic acids.

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