Methyl 6-(((tert-butoxycarbonyl)amino)methyl)nicotinate

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Reagent Code: #203434
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CAS Number 384831-57-6

science Other reagents with same CAS 384831-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.29 g/mol
Formula C₁₃H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD28400841
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of protected amine and ester functionalities. Also utilized in research settings for building nitrogen-containing heterocyclic systems relevant to drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,030.00
inventory 250mg
10-20 days ฿15,350.00
inventory 1g
10-20 days ฿41,420.00
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Methyl 6-(((tert-butoxycarbonyl)amino)methyl)nicotinate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of protected amine and ester functionalities. Also utilized in research settings for building nitrogen-conta

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of protected amine and ester functionalities. Also utilized in research settings for building nitrogen-containing heterocyclic systems relevant to drug discovery.

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