3-Amino-5-fluoro-4-methylbenzoicacid

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Reagent Code: #139417
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CAS Number 103877-75-4

science Other reagents with same CAS 103877-75-4

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scatter_plot Molecular Information
Weight 169.15 g/mol
Formula C₈H₈FNO₂
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MDL Number MFCD09835203
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports enhanced bioavailability and receptor binding due to the combined effects of the fluorine atom and amino group. Also employed in the preparation of agrochemicals, where the methyl and fluoro substituents contribute to improved metabolic stability and target specificity. Additionally, serves as a building block in the manufacture of specialty polymers and fluorescent dyes, leveraging its aromatic backbone and functional groups for cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,880.00
inventory 250mg
10-20 days ฿9,850.00
inventory 1g
10-20 days ฿36,220.00

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3-Amino-5-fluoro-4-methylbenzoicacid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports enhanced bioavailability and receptor binding due to the combined effects of the fluorine atom and amino group. Also employed in the preparation of agrochemicals, where the methyl and fluoro substituents contribute to improved metabolic stability and target specificity. Additionally, s

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports enhanced bioavailability and receptor binding due to the combined effects of the fluorine atom and amino group. Also employed in the preparation of agrochemicals, where the methyl and fluoro substituents contribute to improved metabolic stability and target specificity. Additionally, serves as a building block in the manufacture of specialty polymers and fluorescent dyes, leveraging its aromatic backbone and functional groups for cross-coupling reactions.

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