2-Amino-5-(4-methyl-1-piperazinyl)benzoic Acid

≥95%

Reagent Code: #139182
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CAS Number 835879-06-6

science Other reagents with same CAS 835879-06-6

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scatter_plot Molecular Information
Weight 235.28 g/mol
Formula C₁₂H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD12869794
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. Its structure allows for functionalization that enhances the pharmacokinetic properties of the final drug compounds, including improved solubility and bacterial targeting. Commonly employed in pharmaceutical research and development for optimizing antibiotic efficacy against resistant bacterial strains. Also utilized in the preparation of biologically active molecules in medicinal chemistry due to its amine and carboxylic acid functional groups, which facilitate coupling reactions and molecular diversification.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,130.00

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2-Amino-5-(4-methyl-1-piperazinyl)benzoic Acid
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Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. Its structure allows for functionalization that enhances the pharmacokinetic properties of the final drug compounds, including improved solubility and bacterial targeting. Commonly employed in pharmaceutical research and development for optimizing antibiotic efficacy against resistant bacterial strains. Also utilized in the preparation of biologically active

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. Its structure allows for functionalization that enhances the pharmacokinetic properties of the final drug compounds, including improved solubility and bacterial targeting. Commonly employed in pharmaceutical research and development for optimizing antibiotic efficacy against resistant bacterial strains. Also utilized in the preparation of biologically active molecules in medicinal chemistry due to its amine and carboxylic acid functional groups, which facilitate coupling reactions and molecular diversification.

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