3-(4-Bromophenyl)pyridine

95%

Reagent Code: #145432
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CAS Number 129013-83-8

science Other reagents with same CAS 129013-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.09 g/mol
Formula C₁₁H₈BrN
thermostat Physical Properties
Boiling Point 331.9°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of biologically active compounds, including kinase inhibitors and receptor modulators. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to construct complex aromatic systems. Also utilized in materials science for developing organic semiconductors and luminescent compounds due to its stable aromatic structure and electron-accepting properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿2,710.00
inventory 10g
10-20 days ฿24,820.00
inventory 25g
10-20 days ฿61,880.00
inventory 5g
10-20 days ฿13,180.00

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3-(4-Bromophenyl)pyridine
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of biologically active compounds, including kinase inhibitors and receptor modulators. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to construct complex aromatic systems. Also utilized in materials science for developing organic semiconductors and luminescent compounds due to its stable aromatic structure and electron-accepting properties.

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of biologically active compounds, including kinase inhibitors and receptor modulators. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to construct complex aromatic systems. Also utilized in materials science for developing organic semiconductors and luminescent compounds due to its stable aromatic structure and electron-accepting properties.

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