(3AR,4S,5R,6aS)-5-((tert-butyldiphenylsilyl)oxy)-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one

97%

Reagent Code: #137780
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CAS Number 618386-94-0

science Other reagents with same CAS 618386-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.58 g/mol
Formula C₂₄H₃₀O₄Si
badge Registry Numbers
MDL Number MFCD30471834
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its functional groups and stereochemistry make it valuable for constructing chiral building blocks in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents due to its ability to participate in selective ring-forming reactions. The tert-butyldiphenylsilyl (TBDPS) protecting group allows for controlled reactivity, enabling stepwise transformations in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,120.00
(3AR,4S,5R,6aS)-5-((tert-butyldiphenylsilyl)oxy)-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one
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Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its functional groups and stereochemistry make it valuable for constructing chiral building blocks in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents due to its ability to participate in selective ring-forming reactions. The tert-butyldiphenylsilyl (TBDPS) protecting group allows for controlled reactivity, enabling stepwise transform

Used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its functional groups and stereochemistry make it valuable for constructing chiral building blocks in asymmetric synthesis. Commonly employed in the development of antiviral and anticancer agents due to its ability to participate in selective ring-forming reactions. The tert-butyldiphenylsilyl (TBDPS) protecting group allows for controlled reactivity, enabling stepwise transformations in multi-step synthetic routes.

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