Methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate

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Reagent Code: #207029
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CAS Number 26845-47-6

science Other reagents with same CAS 26845-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.23 g/mol
Formula C₁₀H₁₆O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its spirocyclic structure serves as a protected form of cyclohexanone, allowing selective reactions at other functional sites. Commonly employed in the synthesis of prostaglandins and other complex natural products where controlled ring-opening and ester transformation are required. The compound’s stability and reactivity make it valuable in multi-step synthetic routes, especially in medicinal chemistry for building cyclic frameworks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿460.00
inventory 1g
10-20 days ฿950.00
inventory 5g
10-20 days ฿3,990.00
inventory 25g
10-20 days ฿15,500.00

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Methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its spirocyclic structure serves as a protected form of cyclohexanone, allowing selective reactions at other functional sites. Commonly employed in the synthesis of prostaglandins and other complex natural products where controlled ring-opening and ester transformation are required. The compound’s stability and reactivity make it valuable in multi-step synthetic routes, especially

Used as a key intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its spirocyclic structure serves as a protected form of cyclohexanone, allowing selective reactions at other functional sites. Commonly employed in the synthesis of prostaglandins and other complex natural products where controlled ring-opening and ester transformation are required. The compound’s stability and reactivity make it valuable in multi-step synthetic routes, especially in medicinal chemistry for building cyclic frameworks.

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