[1-(5-BroMo-pyridin-2-yl)-pyrrolidin-3-yl]-carbaMic acid tert-butyl ester

≥95%

Reagent Code: #149727
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CAS Number 1088410-93-8

science Other reagents with same CAS 1088410-93-8

blur_circular Chemical Specifications

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Weight 342.23 g/mol
Formula C₁₄H₂₀BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting specific signaling pathways involved in inflammation and cancer. The tert-butyl carbamate group protects the amine during synthesis, allowing selective deprotection for further functionalization. Commonly applied in medicinal chemistry for optimizing drug candidates due to its stability and compatibility with various coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,420.00
inventory 250mg
10-20 days ฿22,220.00
inventory 1g
10-20 days ฿69,960.00

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[1-(5-BroMo-pyridin-2-yl)-pyrrolidin-3-yl]-carbaMic acid tert-butyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting specific signaling pathways involved in inflammation and cancer. The tert-butyl carbamate group protects the amine during synthesis, allowing selective deprotection for further functionalization. Commonly applied in medicinal chemistry for optimizing drug candidates due to its stability and compatibility

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports the formation of biologically active molecules targeting specific signaling pathways involved in inflammation and cancer. The tert-butyl carbamate group protects the amine during synthesis, allowing selective deprotection for further functionalization. Commonly applied in medicinal chemistry for optimizing drug candidates due to its stability and compatibility with various coupling reactions.

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