4-Ethyl-2-fluorobenzoic acid

≥96%

Reagent Code: #131714
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CAS Number 37135-28-7

science Other reagents with same CAS 37135-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.17 g/mol
Formula C₉H₉FO₂
badge Registry Numbers
MDL Number MFCD18411934
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. Its structure allows for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated aromatic compounds where the fluorine atom influences binding affinity to biological targets. Also utilized in agrochemicals for the production of herbicides and fungicides due to its ability to improve lipophilicity and environmental persistence. Serves as a building block in organic synthesis, especially in cross-coupling reactions and carbonyl derivatizations for fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,130.00
inventory 250mg
10-20 days ฿9,510.00
inventory 1g
10-20 days ฿28,520.00

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4-Ethyl-2-fluorobenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. Its structure allows for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated aromatic compounds where the fluorine atom influences binding affinity to biological targets. Also utilized in agrochemicals for the production of herbic

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. Its structure allows for selective modification in drug design, enhancing metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated aromatic compounds where the fluorine atom influences binding affinity to biological targets. Also utilized in agrochemicals for the production of herbicides and fungicides due to its ability to improve lipophilicity and environmental persistence. Serves as a building block in organic synthesis, especially in cross-coupling reactions and carbonyl derivatizations for fine chemical manufacturing.

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