4′-Hydroxy-biphenyl-2-carbaldehyde

95%

Reagent Code: #130330
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CAS Number 400747-55-9

science Other reagents with same CAS 400747-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.221 g/mol
Formula C₁₃H₁₀O₂
thermostat Physical Properties
Boiling Point 379.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.202±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the formation of biphenyl-based compounds with enhanced binding affinity to biological targets. Also employed in the preparation of liquid crystals and organic semiconductors due to its conjugated aromatic system. Serves as a building block in cross-coupling reactions for creating complex organic frameworks in medicinal and materials chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,860.00

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4′-Hydroxy-biphenyl-2-carbaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the formation of biphenyl-based compounds with enhanced binding affinity to biological targets. Also employed in the preparation of liquid crystals and organic semiconductors due to its conjugated aromatic system. Serves as a building block in cross-coupling reactions for creating complex organic frameworks in

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the formation of biphenyl-based compounds with enhanced binding affinity to biological targets. Also employed in the preparation of liquid crystals and organic semiconductors due to its conjugated aromatic system. Serves as a building block in cross-coupling reactions for creating complex organic frameworks in medicinal and materials chemistry.

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