3'-Chloro-2-fluoro-4'-methyl-[1,1'-biphenyl]-4-carboxylic acid

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Reagent Code: #79437
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CAS Number 1261965-53-0

science Other reagents with same CAS 1261965-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.68 g/mol
Formula C₁₄H₁₀ClFO₂
badge Registry Numbers
MDL Number MFCD18320782
thermostat Physical Properties
Boiling Point 400.2±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex compounds. Its structure, featuring both chloro and fluoro substituents, makes it valuable for developing active pharmaceutical ingredients (APIs) with specific biological activities. It is often employed in the creation of drugs targeting inflammation, cancer, or infectious diseases due to its ability to modulate molecular interactions effectively. In agrochemicals, it serves as a building block for designing herbicides or pesticides, leveraging its aromatic and halogenated properties to enhance efficacy and selectivity. Additionally, its carboxylic acid group allows for further functionalization, making it versatile in organic synthesis and drug discovery processes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,827.00

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3'-Chloro-2-fluoro-4'-methyl-[1,1'-biphenyl]-4-carboxylic acid
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This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex compounds. Its structure, featuring both chloro and fluoro substituents, makes it valuable for developing active pharmaceutical ingredients (APIs) with specific biological activities. It is often employed in the creation of drugs targeting inflammation, cancer, or infectious diseases due to its ability to modulate molecular interactions effectively. In agrochemicals, it serves as a building block for designing herbicides or pesticides, leveraging its aromatic and halogenated properties to enhance efficacy and selectivity. Additionally, its carboxylic acid group allows for further functionalization, making it versatile in organic synthesis and drug discovery processes.
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