1-(5-Bromo-3-nitropyridin-2-YL)ethanone

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Reagent Code: #151276
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CAS Number 1363382-81-3

science Other reagents with same CAS 1363382-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.030 g/mol
Formula C₇H₅BrN₂O₃
badge Registry Numbers
MDL Number MFCD21642002
thermostat Physical Properties
Boiling Point 333.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, dry seal

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 functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in anticancer and anti-inflammatory agents. Also utilized in research settings for designing novel pyridine-based derivatives with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,560.00
inventory 250mg
10-20 days ฿11,800.00

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1-(5-Bromo-3-nitropyridin-2-YL)ethanone
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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 functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in anticancer and anti-inflammatory agents. Also utilized in research settings for designing novel pyridine-based derivatives with

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 functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in anticancer and anti-inflammatory agents. Also utilized in research settings for designing novel pyridine-based derivatives with potential biological activity.

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