tert-Butyl 3-(2-chloronicotinamido)pyrrolidine-1-carboxylate

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Reagent Code: #130066
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CAS Number 1353989-82-8

science Other reagents with same CAS 1353989-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.79 g/mol
Formula C₁₅H₂₀ClN₃O₃
badge Registry Numbers
MDL Number MFCD21098629
thermostat Physical Properties
Boiling Point 484.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.28±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during peptide coupling or sequential reactions, enabling selective functionalization. The chloronicotinamide moiety contributes to binding affinity in receptor interactions, making this compound valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,990.00
inventory 100mg
10-20 days ฿6,470.00

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tert-Butyl 3-(2-chloronicotinamido)pyrrolidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during peptide coupling or sequential reactions, enabling selective functionalization. The chloron

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during peptide coupling or sequential reactions, enabling selective functionalization. The chloronicotinamide moiety contributes to binding affinity in receptor interactions, making this compound valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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