3-Fluoro-5-methylbenzoic acid

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Reagent Code: #187186
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Alias 3-Fluoro-5-methylbenzoic acid
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CAS Number 518070-19-4

science Other reagents with same CAS 518070-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.14 g/mol
Formula C₈H₇FO₂
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EC Number None
MDL Number MFCD03094313
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs and anti-inflammatory agents. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in drug molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other neuroactive compounds. Also utilized in agrochemicals for the production of herbicides and fungicides due to its ability to improve lipophilicity and target binding in biologically active molecules. Serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies involving fluorinated analogs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28.00
inventory 25g
10-20 days ฿2,310.00
inventory 100g
10-20 days ฿9,220.00
inventory 5g
10-20 days ฿55.00
3-Fluoro-5-methylbenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs and anti-inflammatory agents. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in drug molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other neuroactive compounds. Also utilized in agrochemicals for the production of herbicides and fungicides due to its ability to improve lipophilicity and target binding in biologically active molecules. Serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies involving fluorinated analogs.
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