1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-1,2,3-triazole-4-carboxylic acid

95%

Reagent Code: #39096
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CAS Number 1119452-31-1

science Other reagents with same CAS 1119452-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.3223 g/mol
Formula C₁₃H₂₀N₄O₄
badge Registry Numbers
MDL Number MFCD12027299
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperidine ring and a triazole moiety, makes it a valuable building block for the development of pharmaceuticals, particularly in the design of protease inhibitors and other enzyme-targeting drugs. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the creation of complex drug candidates. Additionally, its carboxylic acid functionality provides a versatile handle for further chemical modifications, such as amide bond formation, which is crucial in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,120.00
inventory 100mg
10-20 days ฿3,030.00
inventory 1g
10-20 days ฿10,290.00
inventory 10g
10-20 days ฿70,190.00
inventory 5g
10-20 days ฿35,100.00

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1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-1,2,3-triazole-4-carboxylic acid
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperidine ring and a triazole moiety, makes it a valuable building block for the development of pharmaceuticals, particularly in the design of protease inhibitors and other enzyme-targeting drugs. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the c

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperidine ring and a triazole moiety, makes it a valuable building block for the development of pharmaceuticals, particularly in the design of protease inhibitors and other enzyme-targeting drugs. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the creation of complex drug candidates. Additionally, its carboxylic acid functionality provides a versatile handle for further chemical modifications, such as amide bond formation, which is crucial in drug discovery and development.

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