(R)-tert-Butyl 2-(dimethylcarbamoyl)piperazine-1-carboxylate hydrochloride

95%

Reagent Code: #231161
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CAS Number 1217825-46-1

science Other reagents with same CAS 1217825-46-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.79 g/mol
Formula C₁₂H₂₄ClN₃O₃
badge Registry Numbers
MDL Number MFCD11112292
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperazine structure with a dimethylcarbamoyl group enables selective reactions in multi-step organic syntheses, especially in the production of central nervous system agents and kinase inhibitors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,220.00
inventory 250mg
10-20 days ฿22,230.00
inventory 1g
10-20 days ฿55,010.00
(R)-tert-Butyl 2-(dimethylcarbamoyl)piperazine-1-carboxylate hydrochloride
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperazine structure with a dimethylcarbamoyl group enables selective reactions in multi-step organic syntheses, especially in the production of central nervous system agents and kinase inhibitors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereoc

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperazine structure with a dimethylcarbamoyl group enables selective reactions in multi-step organic syntheses, especially in the production of central nervous system agents and kinase inhibitors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.

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