2-(4-(tert-Butoxycarbonyl)-3-(methoxycarbonyl)piperazin-1-yl)acetic acid

95%

Reagent Code: #130887
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CAS Number 1353945-18-2

science Other reagents with same CAS 1353945-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.32 g/mol
Formula C₁₃H₂₂N₂O₆
badge Registry Numbers
MDL Number MFCD21096818
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other bioactive molecules. Its piperazine core with two ester functionalities allows selective modifications, enabling controlled introduction of substituents during multi-step syntheses. The tert-butoxycarbonyl (Boc) group provides effective amine protection, while the methoxycarbonyl and acetic acid moieties offer sites for peptide coupling or further functionalization. It is especially valuable in medicinal chemistry for constructing complex heterocyclic systems with high purity and yield.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,760.00
inventory 1g
10-20 days ฿113,600.00
inventory 250mg
10-20 days ฿42,090.00

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2-(4-(tert-Butoxycarbonyl)-3-(methoxycarbonyl)piperazin-1-yl)acetic acid
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Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other bioactive molecules. Its piperazine core with two ester functionalities allows selective modifications, enabling controlled introduction of substituents during multi-step syntheses. The tert-butoxycarbonyl (Boc) group provides effective amine protection, while the methoxycarbonyl and acetic acid moieti

Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other bioactive molecules. Its piperazine core with two ester functionalities allows selective modifications, enabling controlled introduction of substituents during multi-step syntheses. The tert-butoxycarbonyl (Boc) group provides effective amine protection, while the methoxycarbonyl and acetic acid moieties offer sites for peptide coupling or further functionalization. It is especially valuable in medicinal chemistry for constructing complex heterocyclic systems with high purity and yield.

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