(4S,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,4-diyl diacetate

95%

Reagent Code: #235165
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CAS Number 4594-52-9

science Other reagents with same CAS 4594-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.25 g/mol
Formula C₁₁H₁₆O₇
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as a chiral building block for the preparation of complex natural products and pharmaceuticals. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of bioactive molecules such as antiviral or anticancer agents. Commonly employed in the construction of polyketide-like structures and sugar analogs due to its functionalized tetrahydrofuran core and protected hydroxyl groups. The acetate groups allow for selective deprotection and further derivatization, enabling its use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,490.00
(4S,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,4-diyl diacetate
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Used in organic synthesis as a chiral building block for the preparation of complex natural products and pharmaceuticals. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of bioactive molecules such as antiviral or anticancer agents. Commonly employed in the construction of polyketide-like structures and sugar analogs due to its functionalized tetrahydrofuran core and protected hydroxyl groups. The acetate groups allow for selective deprotection and further d

Used in organic synthesis as a chiral building block for the preparation of complex natural products and pharmaceuticals. Its stereochemistry makes it valuable in asymmetric synthesis, particularly in the development of bioactive molecules such as antiviral or anticancer agents. Commonly employed in the construction of polyketide-like structures and sugar analogs due to its functionalized tetrahydrofuran core and protected hydroxyl groups. The acetate groups allow for selective deprotection and further derivatization, enabling its use in multi-step synthetic routes.

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