(R)-Benzyl 3-methylpiperazine-1-carboxylate hydrochloride

≥95%

Reagent Code: #113571
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CAS Number 1217831-52-1

science Other reagents with same CAS 1217831-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.76 g/mol
Formula C₁₃H₁₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD09029383
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its chiral nature makes it valuable in the creation of enantiomerically pure substances, which are critical in the development of drugs with specific therapeutic effects and reduced side effects. Additionally, it is employed in organic synthesis to construct complex molecular structures, often contributing to the study of receptor-ligand interactions and the optimization of drug efficacy. Its hydrochloride form enhances stability and solubility, making it more practical for use in laboratory settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,592.00
inventory 100mg
10-20 days ฿522.00
inventory 250mg
10-20 days ฿873.00

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(R)-Benzyl 3-methylpiperazine-1-carboxylate hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its chiral nature makes it valuable in the creation of enantiomerically pure substances, which are critical in the development of drugs with specific therapeutic effects and reduced side effects. Additionally, it is employed in organic synthesis to

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its chiral nature makes it valuable in the creation of enantiomerically pure substances, which are critical in the development of drugs with specific therapeutic effects and reduced side effects. Additionally, it is employed in organic synthesis to construct complex molecular structures, often contributing to the study of receptor-ligand interactions and the optimization of drug efficacy. Its hydrochloride form enhances stability and solubility, making it more practical for use in laboratory settings.

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