8-Nitro-1,4-Dioxaspiro[4.5]Decane

95%

Reagent Code: #219081
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CAS Number 635728-10-8

science Other reagents with same CAS 635728-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.19 g/mol
Formula C₈H₁₃NO₄
badge Registry Numbers
MDL Number MFCD27998098
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and nitro-containing compounds. Its spirocyclic structure with a nitro functional group makes it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in research settings to explore new synthetic pathways and to prepare derivatives with potential antimicrobial or anti-inflammatory properties. The compound's stability and reactivity profile allow for selective transformations, making it useful in the design of novel drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,940.00

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8-Nitro-1,4-Dioxaspiro[4.5]Decane
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and nitro-containing compounds. Its spirocyclic structure with a nitro functional group makes it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in research settings to explore new synthetic pathways and to prepare derivatives with potential antimicrobial or anti-inflammatory properties. The compound's stability and reactivity profile allow

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and nitro-containing compounds. Its spirocyclic structure with a nitro functional group makes it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in research settings to explore new synthetic pathways and to prepare derivatives with potential antimicrobial or anti-inflammatory properties. The compound's stability and reactivity profile allow for selective transformations, making it useful in the design of novel drug candidates.

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