2-(1,4-Bis(tert-butoxycarbonyl)piperazin-2-yl)acetic acid

97%

Reagent Code: #41203
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CAS Number 368442-00-6

science Other reagents with same CAS 368442-00-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.4033 g/mol
Formula C₁₆H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD07776825
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate. It plays a crucial role in the development of complex molecules, particularly in the construction of piperazine derivatives, which are often found in bioactive compounds and drugs. Its tert-butoxycarbonyl (Boc) protecting groups make it valuable in peptide synthesis, allowing for selective deprotection and modification during multi-step reactions. Additionally, it is employed in the preparation of ligands for catalysis and in the study of enzyme inhibitors, contributing to advancements in medicinal chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,909.00
2-(1,4-Bis(tert-butoxycarbonyl)piperazin-2-yl)acetic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate. It plays a crucial role in the development of complex molecules, particularly in the construction of piperazine derivatives, which are often found in bioactive compounds and drugs. Its tert-butoxycarbonyl (Boc) protecting groups make it valuable in peptide synthesis, allowing for selective deprotection and modification during multi-step reactions. Additionally, it is employed in the preparation of lig

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate. It plays a crucial role in the development of complex molecules, particularly in the construction of piperazine derivatives, which are often found in bioactive compounds and drugs. Its tert-butoxycarbonyl (Boc) protecting groups make it valuable in peptide synthesis, allowing for selective deprotection and modification during multi-step reactions. Additionally, it is employed in the preparation of ligands for catalysis and in the study of enzyme inhibitors, contributing to advancements in medicinal chemistry and drug discovery.

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