tert-butyl 4-(2-amino-2-oxoethyl)-3-oxopiperazine-1-carboxylate

≥95%

Reagent Code: #244713
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CAS Number 1951451-63-0

science Other reagents with same CAS 1951451-63-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.29 g/mol
Formula C₁₁H₁₉N₃O₄
badge Registry Numbers
MDL Number MFCD28506272
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving piperazine scaffolds. Its structure allows for selective modifications, making it valuable in drug discovery for introducing functionalized amino acid-like moieties. Commonly employed in the preparation of peptide mimetics and nitrogen-containing heterocycles with biological activity. Suitable for solid-phase and solution-phase peptide synthesis due to the presence of orthogonal protecting groups. Also applied in the production of kinase inhibitors and antimicrobial agents during medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿57,000.00
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tert-butyl 4-(2-amino-2-oxoethyl)-3-oxopiperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving piperazine scaffolds. Its structure allows for selective modifications, making it valuable in drug discovery for introducing functionalized amino acid-like moieties. Commonly employed in the preparation of peptide mimetics and nitrogen-containing heterocycles with biological activity. Suitable for solid-phase and solution-phase peptide synthesis due t

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) involving piperazine scaffolds. Its structure allows for selective modifications, making it valuable in drug discovery for introducing functionalized amino acid-like moieties. Commonly employed in the preparation of peptide mimetics and nitrogen-containing heterocycles with biological activity. Suitable for solid-phase and solution-phase peptide synthesis due to the presence of orthogonal protecting groups. Also applied in the production of kinase inhibitors and antimicrobial agents during medicinal chemistry research.

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