3-HYDROXYMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

95%

Reagent Code: #193810
label
Alias tert-butyl 3-hydroxymethylpiperazine-1-carboxylate
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CAS Number 301673-16-5

science Other reagents with same CAS 301673-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD04115304
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine moieties. Its protected functional groups allow selective reactions in multi-step organic syntheses, especially in the production of kinase inhibitors, antiviral agents, and central nervous system (CNS) drugs. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide-like synthesis. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate solubility, bioavailability, and binding affinity.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿132.00
inventory 1g
10-20 days ฿170.50
inventory 25g
10-20 days ฿4,120.00
inventory 5g
10-20 days ฿1,150.00

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3-HYDROXYMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine moieties. Its protected functional groups allow selective reactions in multi-step organic syntheses, especially in the production of kinase inhibitors, antiviral agents, and central nervous system (CNS) drugs. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide-like synthesis. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate solubility, bioavailability, and binding affinity.
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