1,1':3',1''-Terphenyl, 4-bromo-

≥95%

Reagent Code: #240247
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CAS Number 54590-37-3

science Other reagents with same CAS 54590-37-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.20 g/mol
Formula C₁₈H₁₃Br
badge Registry Numbers
MDL Number MFCD20486761
thermostat Physical Properties
Melting Point 90-95°C
Boiling Point 421.5±14.0 °C(Predicted)
inventory_2 Storage & Handling
Density 421.5±14.0 °C(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of liquid crystals and advanced materials. It serves as a building block in the development of organic semiconductors and electroluminescent compounds for OLEDs. The bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Also employed in the synthesis of pharmaceuticals and agrochemicals where extended aromatic frameworks are required. Its rigid terphenyl backbone contributes to thermal stability and structural control in supramolecular chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,140.00
inventory 25g
10-20 days ฿15,260.00
inventory 5g
10-20 days ฿3,930.00

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1,1':3',1''-Terphenyl, 4-bromo-
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Used as an intermediate in organic synthesis, particularly in the preparation of liquid crystals and advanced materials. It serves as a building block in the development of organic semiconductors and electroluminescent compounds for OLEDs. The bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Also employed in the synthesis of pharmaceuticals and agrochemicals where extended aromatic frameworks are re

Used as an intermediate in organic synthesis, particularly in the preparation of liquid crystals and advanced materials. It serves as a building block in the development of organic semiconductors and electroluminescent compounds for OLEDs. The bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Also employed in the synthesis of pharmaceuticals and agrochemicals where extended aromatic frameworks are required. Its rigid terphenyl backbone contributes to thermal stability and structural control in supramolecular chemistry.

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