4-Hydroxy-6-Methylquinoline-3-Carboxylic Acid

98%

Reagent Code: #197167
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CAS Number 35973-18-3

science Other reagents with same CAS 35973-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of quinolone-based antibiotics and other bioactive compounds, particularly in the development of antimicrobial agents effective against bacterial infections. The 4-hydroxyquinoline-3-carboxylic acid structure serves as a scaffold for introducing fluoro or other substituents to enhance potency against Gram-negative and Gram-positive bacteria. It is also employed in research for anticancer agents due to its metal-chelating properties and interactions with biological targets. Additionally, its conjugated system supports applications in materials science, such as fluorescent dyes or organocatalysts in organic synthesis. The compound facilitates structure-activity relationship studies through facile derivatization at multiple positions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿5,000.00
1g
10-20 days ฿8,600.00
100mg
10-20 days ฿2,500.00
4-Hydroxy-6-Methylquinoline-3-Carboxylic Acid
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Used as a key intermediate in the synthesis of quinolone-based antibiotics and other bioactive compounds, particularly in the development of antimicrobial agents effective against bacterial infections. The 4-hydroxyquinoline-3-carboxylic acid structure serves as a scaffold for introducing fluoro or other substituents to enhance potency against Gram-negative and Gram-positive bacteria. It is also employed in research for anticancer agents due to its metal-chelating properties and interactions with biologi

Used as a key intermediate in the synthesis of quinolone-based antibiotics and other bioactive compounds, particularly in the development of antimicrobial agents effective against bacterial infections. The 4-hydroxyquinoline-3-carboxylic acid structure serves as a scaffold for introducing fluoro or other substituents to enhance potency against Gram-negative and Gram-positive bacteria. It is also employed in research for anticancer agents due to its metal-chelating properties and interactions with biological targets. Additionally, its conjugated system supports applications in materials science, such as fluorescent dyes or organocatalysts in organic synthesis. The compound facilitates structure-activity relationship studies through facile derivatization at multiple positions.

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