2-Amino-5-fluoro-3-methylbenzoic acid

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Reagent Code: #61778
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CAS Number 874804-25-8

science Other reagents with same CAS 874804-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.15 g/mol
Formula C₈H₈FNO₂
badge Registry Numbers
MDL Number MFCD06409107
inventory_2 Storage & Handling
Storage Room temperature, avoid light, store in inert gas

description Product Description

2-Amino-5-fluoro-3-methylbenzoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both amino and carboxylic acid functional groups, makes it a versatile building block for the development of drugs, particularly those targeting specific biological pathways. It is often employed in the production of compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its fluorine substituent enhances the metabolic stability and bioavailability of the resulting drug molecules, making it a valuable component in medicinal chemistry research and drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,764.00
inventory 250mg
10-20 days ฿2,979.00
inventory 1g
10-20 days ฿8,046.00

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2-Amino-5-fluoro-3-methylbenzoic acid
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2-Amino-5-fluoro-3-methylbenzoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both amino and carboxylic acid functional groups, makes it a versatile building block for the development of drugs, particularly those targeting specific biological pathways. It is often employed in the production of compounds with potential anti-inflammatory, antimicrobial, or anticancer properties.

2-Amino-5-fluoro-3-methylbenzoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both amino and carboxylic acid functional groups, makes it a versatile building block for the development of drugs, particularly those targeting specific biological pathways. It is often employed in the production of compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its fluorine substituent enhances the metabolic stability and bioavailability of the resulting drug molecules, making it a valuable component in medicinal chemistry research and drug design.

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