7-Chloro-6-nitrofuro[3,2-b]pyridine

95%

Reagent Code: #142241
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CAS Number 2222137-89-3

science Other reagents with same CAS 2222137-89-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.56 g/mol
Formula C₇H₃ClN₂O₃
thermostat Physical Properties
Boiling Point 288.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.609±0.06 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 antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing properties and ability to enhance binding affinity. Also utilized in the preparation of fluorescent probes and agrochemicals owing to its reactivity and stability under various coupling conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,360.00
inventory 250mg
10-20 days ฿7,400.00
inventory 1g
10-20 days ฿19,990.00
7-Chloro-6-nitrofuro[3,2-b]pyridine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing properties and ability to enhance binding affinity. Also utilized in the preparation of fluorescent probes and ag

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing properties and ability to enhance binding affinity. Also utilized in the preparation of fluorescent probes and agrochemicals owing to its reactivity and stability under various coupling conditions.

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