4-Amino-2-(trifluoromethyl)benzoic acid

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Reagent Code: #135024
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CAS Number 393-06-6

science Other reagents with same CAS 393-06-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.14 g/mol
Formula C₈H₆F₃NO₂
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MDL Number MFCD03407959
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amino and carboxylic acid functional groups, which allow for easy derivatization. Commonly employed in the preparation of amide and ester derivatives for drug discovery research. Also utilized in the synthesis of agrochemicals and fluorescent dyes where the trifluoromethyl group enhances stability and lipophilicity. Its structural features make it valuable in medicinal chemistry for optimizing pharmacokinetic properties of new chemical entities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿800.00
inventory 25g
10-20 days ฿3,280.00
inventory 100g
10-20 days ฿12,280.00

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4-Amino-2-(trifluoromethyl)benzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amino and carboxylic acid functional groups, which allow for easy derivatization. Commonly employed in the preparation of amide and ester derivatives for drug discovery research. Also utilized in the synthesis of agrochemi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in the development of bioactive molecules due to the presence of both amino and carboxylic acid functional groups, which allow for easy derivatization. Commonly employed in the preparation of amide and ester derivatives for drug discovery research. Also utilized in the synthesis of agrochemicals and fluorescent dyes where the trifluoromethyl group enhances stability and lipophilicity. Its structural features make it valuable in medicinal chemistry for optimizing pharmacokinetic properties of new chemical entities.

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