1-Boc-3-Carbamoylpiperazine

98%

Reagent Code: #72284
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CAS Number 112257-24-6

science Other reagents with same CAS 112257-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.28 g/mol
Formula C₁₀H₁₉N₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used extensively in pharmaceutical synthesis, it serves as a key intermediate in the production of various drugs, particularly those targeting the central nervous system. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and the development of bioactive compounds. It is also employed in the creation of kinase inhibitors and other small molecules with therapeutic potential. The carbamoyl group enhances its utility in forming stable amide bonds, essential for constructing complex molecular structures in medicinal chemistry.

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Test Parameter Specification
Appearance White to Off-white to Light brown Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿855.00
inventory 100mg
10-20 days ฿1,512.00

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1-Boc-3-Carbamoylpiperazine
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Used extensively in pharmaceutical synthesis, it serves as a key intermediate in the production of various drugs, particularly those targeting the central nervous system. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and the development of bioactive compounds. It is also employed in the creation of kinase inhibitors and other small molecules with therapeutic potential. The carbamoyl group enhances its utility in forming stable amide bonds, essential

Used extensively in pharmaceutical synthesis, it serves as a key intermediate in the production of various drugs, particularly those targeting the central nervous system. Its Boc-protected amine group allows for selective reactions, making it valuable in peptide coupling and the development of bioactive compounds. It is also employed in the creation of kinase inhibitors and other small molecules with therapeutic potential. The carbamoyl group enhances its utility in forming stable amide bonds, essential for constructing complex molecular structures in medicinal chemistry.

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