3-Chloro-4-(4-fluorophenoxy)aniline

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Reagent Code: #165258
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CAS Number 937608-56-5

science Other reagents with same CAS 937608-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.66 g/mol
Formula C₁₂H₉ClFNO
badge Registry Numbers
MDL Number MFCD08687313
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its aromatic structure and reactive amine group. Its fluorophenoxy and chloro substituents enhance bioactivity and stability, making it valuable in developing crop protection agents. Also employed in pharmaceutical research for constructing biologically active molecules, especially those targeting enzyme inhibition or receptor modulation. The compound's ability to participate in coupling reactions supports its use in creating complex organic molecules for drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿500.00
inventory 250mg
10-20 days ฿1,020.00

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3-Chloro-4-(4-fluorophenoxy)aniline
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its aromatic structure and reactive amine group. Its fluorophenoxy and chloro substituents enhance bioactivity and stability, making it valuable in developing crop protection agents. Also employed in pharmaceutical research for constructing biologically active molecules, especially those targeting enzyme inhibition or receptor modulation. The compound's ability to participate in coupling reactio

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its aromatic structure and reactive amine group. Its fluorophenoxy and chloro substituents enhance bioactivity and stability, making it valuable in developing crop protection agents. Also employed in pharmaceutical research for constructing biologically active molecules, especially those targeting enzyme inhibition or receptor modulation. The compound's ability to participate in coupling reactions supports its use in creating complex organic molecules for drug discovery and material science.

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