cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylicacidtert-butylester

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Reagent Code: #179643
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CAS Number 1005397-64-7

science Other reagents with same CAS 1005397-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3 g/mol
Formula C₁₂H₂₁NO₃
badge Registry Numbers
MDL Number MFCD19230167
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl ester group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide-like and medicinal chemistry applications. The compound's stereochemistry (cis configuration) is critical for achieving desired biological activity in target molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,840.00
inventory 250mg
10-20 days ฿20,580.00
inventory 1g
10-20 days ฿51,400.00

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cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylicacidtert-butylester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl ester group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide-like and medicinal chemistry applications. The compound's stereochemistry

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl ester group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide-like and medicinal chemistry applications. The compound's stereochemistry (cis configuration) is critical for achieving desired biological activity in target molecules.

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