1,7-Diazaspiro[4.5]decane-7-carboxylic acid, 2-oxo-, 1,1-diMethylethyl ester

98%

Reagent Code: #42486
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CAS Number 1158749-85-9

science Other reagents with same CAS 1158749-85-9

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Weight 254.33 g/mol
Formula C₁₃H₂₂N₂O₃
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description Product Description

This compound is primarily utilized in organic synthesis as a building block or intermediate for the development of more complex molecules. Its unique spirocyclic structure makes it valuable in the design of pharmaceuticals, particularly in the creation of compounds with potential biological activity. It is often employed in medicinal chemistry research to explore new drug candidates, especially those targeting neurological or metabolic disorders. Additionally, its ester group enhances its stability and reactivity, making it suitable for use in peptide coupling reactions and other synthetic processes. The compound’s structural features also contribute to its application in the study of enzyme inhibitors and receptor modulators.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿33,120.00
inventory 100mg
10-20 days ฿19,899.00
inventory 1g
10-20 days ฿66,339.00

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1,7-Diazaspiro[4.5]decane-7-carboxylic acid, 2-oxo-, 1,1-diMethylethyl ester
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This compound is primarily utilized in organic synthesis as a building block or intermediate for the development of more complex molecules. Its unique spirocyclic structure makes it valuable in the design of pharmaceuticals, particularly in the creation of compounds with potential biological activity. It is often employed in medicinal chemistry research to explore new drug candidates, especially those targeting neurological or metabolic disorders. Additionally, its ester group enhances its stability and

This compound is primarily utilized in organic synthesis as a building block or intermediate for the development of more complex molecules. Its unique spirocyclic structure makes it valuable in the design of pharmaceuticals, particularly in the creation of compounds with potential biological activity. It is often employed in medicinal chemistry research to explore new drug candidates, especially those targeting neurological or metabolic disorders. Additionally, its ester group enhances its stability and reactivity, making it suitable for use in peptide coupling reactions and other synthetic processes. The compound’s structural features also contribute to its application in the study of enzyme inhibitors and receptor modulators.

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