1,2-Bis(4-bromophenyl)ethyne

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Reagent Code: #145611
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CAS Number 2789-89-1

science Other reagents with same CAS 2789-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.02 g/mol
Formula C₁₄H₈Br₂
thermostat Physical Properties
Melting Point 182°C
Boiling Point 383.6°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 conjugated materials for optoelectronic devices such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic transistors. The bromine groups allow further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings, enabling the construction of complex aromatic systems and extended conjugated structures. Also employed in the development of liquid crystals and nonlinear optical materials due to its rigid, planar structure and electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿340.00
inventory 1g
10-20 days ฿910.00
inventory 5g
10-20 days ฿4,180.00
inventory 25g
10-20 days ฿17,760.00
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1,2-Bis(4-bromophenyl)ethyne
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of conjugated materials for optoelectronic devices such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic transistors. The bromine groups allow further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings, enabling the construction of complex aromatic systems and extended conjugated structures. Also employed in t

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of conjugated materials for optoelectronic devices such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic transistors. The bromine groups allow further functionalization via cross-coupling reactions like Suzuki or Sonogashira couplings, enabling the construction of complex aromatic systems and extended conjugated structures. Also employed in the development of liquid crystals and nonlinear optical materials due to its rigid, planar structure and electronic properties.

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