ethyl 4-hydroxy-4-methyl-1-oxa-9-azaspiro[5.5]undecane-9-carboxylate

95%

Reagent Code: #75609
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CAS Number 1785761-67-2

science Other reagents with same CAS 1785761-67-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257 g/mol
Formula C₁₃H₂₃NO₄
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MDL Number MFCD27996022
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly those with potential therapeutic applications. Its unique spirocyclic structure makes it valuable for constructing bioactive compounds, especially in the design of drugs targeting neurological disorders. Researchers often employ it in the synthesis of novel compounds to explore their pharmacological properties, such as receptor binding affinity or enzyme inhibition. Additionally, it may be used in the preparation of chiral catalysts or ligands for asymmetric synthesis, aiding in the production of enantiomerically pure substances. Its versatility in chemical transformations makes it a valuable tool in medicinal chemistry and drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿39,123.00

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ethyl 4-hydroxy-4-methyl-1-oxa-9-azaspiro[5.5]undecane-9-carboxylate
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This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly those with potential therapeutic applications. Its unique spirocyclic structure makes it valuable for constructing bioactive compounds, especially in the design of drugs targeting neurological disorders. Researchers often employ it in the synthesis of novel compounds to explore their pharmacological properties, such as receptor binding affinity or enzyme inhibition. Additionally, it may be used in the preparation of chiral catalysts or ligands for asymmetric synthesis, aiding in the production of enantiomerically pure substances. Its versatility in chemical transformations makes it a valuable tool in medicinal chemistry and drug discovery efforts.
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