(3aR,5S,5aR,8aS,8bR)-2,2,7,7-Tetramethyltetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran-5-carboxylic acid

95%

Reagent Code: #231827
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CAS Number 25253-46-7

science Other reagents with same CAS 25253-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.27 g/mol
Formula C₁₂H₁₈O₇
badge Registry Numbers
MDL Number MFCD06657642
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a chiral building block for the development of complex natural products and pharmaceuticals. Its rigid, polycyclic structure with multiple stereocenters makes it valuable in asymmetric synthesis, particularly in the design of catalysts or intermediates for bioactive molecules. The compound’s functional groups allow for selective modifications, enabling its incorporation into larger molecular frameworks. It is also employed in research related to stereoselective reactions, including cyclizations and carbon–carbon bond-forming processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,220.00
inventory 250mg
10-20 days ฿13,960.00
inventory 1g
10-20 days ฿46,270.00

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(3aR,5S,5aR,8aS,8bR)-2,2,7,7-Tetramethyltetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran-5-carboxylic acid
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Used in organic synthesis as a chiral building block for the development of complex natural products and pharmaceuticals. Its rigid, polycyclic structure with multiple stereocenters makes it valuable in asymmetric synthesis, particularly in the design of catalysts or intermediates for bioactive molecules. The compound’s functional groups allow for selective modifications, enabling its incorporation into larger molecular frameworks. It is also employed in research related to stereoselective reactions, inc

Used in organic synthesis as a chiral building block for the development of complex natural products and pharmaceuticals. Its rigid, polycyclic structure with multiple stereocenters makes it valuable in asymmetric synthesis, particularly in the design of catalysts or intermediates for bioactive molecules. The compound’s functional groups allow for selective modifications, enabling its incorporation into larger molecular frameworks. It is also employed in research related to stereoselective reactions, including cyclizations and carbon–carbon bond-forming processes.

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