(3aR,5R,5aS,8aS,8bR)-5-ethyl-2,2,7,7-tetramethyltetrahydro-3aH-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran

95%

Reagent Code: #230908
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CAS Number 117475-49-7

science Other reagents with same CAS 117475-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.31 g/mol
Formula C₁₃H₂₂O₅
badge Registry Numbers
MDL Number MFCD28405169
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as a chiral building block for the preparation of complex natural products and bioactive molecules. Its rigid polycyclic structure and multiple stereocenters make it valuable in asymmetric synthesis and pharmaceutical research, particularly in the development of stereoselective catalysts or intermediates for drug discovery. The compound’s dioxolane and pyran rings provide stability and specific spatial orientation, useful in designing enzyme inhibitors or receptor ligands.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,800.00
inventory 250mg
10-20 days ฿13,000.00
inventory 1g
10-20 days ฿26,000.00
(3aR,5R,5aS,8aS,8bR)-5-ethyl-2,2,7,7-tetramethyltetrahydro-3aH-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran
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Used in organic synthesis as a chiral building block for the preparation of complex natural products and bioactive molecules. Its rigid polycyclic structure and multiple stereocenters make it valuable in asymmetric synthesis and pharmaceutical research, particularly in the development of stereoselective catalysts or intermediates for drug discovery. The compound’s dioxolane and pyran rings provide stability and specific spatial orientation, useful in designing enzyme inhibitors or receptor ligands.

Used in organic synthesis as a chiral building block for the preparation of complex natural products and bioactive molecules. Its rigid polycyclic structure and multiple stereocenters make it valuable in asymmetric synthesis and pharmaceutical research, particularly in the development of stereoselective catalysts or intermediates for drug discovery. The compound’s dioxolane and pyran rings provide stability and specific spatial orientation, useful in designing enzyme inhibitors or receptor ligands.

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