2-(3-Bromophenyl)-4,6-diphenylpyrimidine

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Reagent Code: #148073
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CAS Number 864377-22-0

science Other reagents with same CAS 864377-22-0

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scatter_plot Molecular Information
Weight 387.2719 g/mol
Formula C₂₂H₁₅BrN₂
badge Registry Numbers
MDL Number MFCD29477691
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and organic electronic materials. Its structure supports conjugation and electron transport, making it valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Also employed in research for creating novel heterocyclic compounds with potential biological activity, including kinase inhibitors and anti-cancer agents. Its bromine functionality allows for further modification via cross-coupling reactions, enabling diverse chemical derivatization for drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿3,260.00
inventory 5g
10-20 days ฿12,300.00
inventory 25g
10-20 days ฿45,670.00

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2-(3-Bromophenyl)-4,6-diphenylpyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals and organic electronic materials. Its structure supports conjugation and electron transport, making it valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Also employed in research for creating novel heterocyclic compounds with potential biological activity, including kinase inhibitors and anti-cancer agents. Its bromine functionality allows for further modification via cross-coupling reactio

Used as a key intermediate in the synthesis of pharmaceuticals and organic electronic materials. Its structure supports conjugation and electron transport, making it valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Also employed in research for creating novel heterocyclic compounds with potential biological activity, including kinase inhibitors and anti-cancer agents. Its bromine functionality allows for further modification via cross-coupling reactions, enabling diverse chemical derivatization for drug discovery and material science.

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