Tert-butyl4-(1-hydroxy-2-methylpropan-2-yl)piperazine-1-carboxylate

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Reagent Code: #244408
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CAS Number 955979-01-8

science Other reagents with same CAS 955979-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.36 g/mol
Formula C₁₃H₂₆N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine scaffolds. Its protected piperazine structure allows for selective reactions at other functional groups, making it valuable in multi-step organic syntheses. The hydroxyl and tert-butyl carbamate groups enable further chemical modifications, facilitating the creation of drug candidates targeting central nervous system disorders and metabolic diseases. Commonly employed in research settings for structure-activity relationship (SAR) studies due to its ability to modulate solubility and bioavailability in lead compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,330.00
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Tert-butyl4-(1-hydroxy-2-methylpropan-2-yl)piperazine-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) that require piperazine scaffolds. Its protected piperazine structure allows for selective reactions at other functional groups, making it valuable in multi-step organic syntheses. The hydroxyl and tert-butyl carbamate groups enable further chemical modifications, facilitating the creation of drug candidates targeting central nervous system disorders and metabo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine scaffolds. Its protected piperazine structure allows for selective reactions at other functional groups, making it valuable in multi-step organic syntheses. The hydroxyl and tert-butyl carbamate groups enable further chemical modifications, facilitating the creation of drug candidates targeting central nervous system disorders and metabolic diseases. Commonly employed in research settings for structure-activity relationship (SAR) studies due to its ability to modulate solubility and bioavailability in lead compounds.

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