1-Boc-3-(methylaminomethyl)-pyrrolidine

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Reagent Code: #152461
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CAS Number 404594-16-7

science Other reagents with same CAS 404594-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.305 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD11616685
thermostat Physical Properties
Boiling Point 281.8 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.004 g/cm3
Storage 2-8°C, avoiding light

description Product Description

Used in pharmaceutical synthesis as a protected intermediate for developing active pharmaceutical ingredients (APIs), particularly in the production of kinase inhibitors and central nervous system agents. The Boc-protected amine group allows selective reactivity, while the methylaminomethyl functionality serves as a key linker for further derivatization. Commonly employed in solid-phase and solution-phase peptide-like synthesis where controlled deprotection and coupling are required. Its structural rigidity supports conformational optimization in drug candidates targeting neurological disorders and inflammatory conditions.

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inventory 1g
10-20 days ฿32,600.00

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1-Boc-3-(methylaminomethyl)-pyrrolidine
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Used in pharmaceutical synthesis as a protected intermediate for developing active pharmaceutical ingredients (APIs), particularly in the production of kinase inhibitors and central nervous system agents. The Boc-protected amine group allows selective reactivity, while the methylaminomethyl functionality serves as a key linker for further derivatization. Commonly employed in solid-phase and solution-phase peptide-like synthesis where controlled deprotection and coupling are required. Its structural rigid

Used in pharmaceutical synthesis as a protected intermediate for developing active pharmaceutical ingredients (APIs), particularly in the production of kinase inhibitors and central nervous system agents. The Boc-protected amine group allows selective reactivity, while the methylaminomethyl functionality serves as a key linker for further derivatization. Commonly employed in solid-phase and solution-phase peptide-like synthesis where controlled deprotection and coupling are required. Its structural rigidity supports conformational optimization in drug candidates targeting neurological disorders and inflammatory conditions.

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