8-Chloro-4-hydroxyquinoline-3-carboxylic acid

98%

Reagent Code: #129448
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CAS Number 35966-16-6

science Other reagents with same CAS 35966-16-6

blur_circular Chemical Specifications

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Weight 223.61 g/mol
Formula C₁₀H₆ClNO₃
inventory_2 Storage & Handling
Density 1.6 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. It plays a key role in constructing the core quinoline structure essential for antibacterial activity. Its functional groups allow for selective modifications, enabling the development of compounds with enhanced potency, solubility, and pharmacokinetic properties. Also investigated for its potential in metal chelation and as a building block in medicinal chemistry research targeting enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,310.00
inventory 250mg
10-20 days ฿8,610.00

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8-Chloro-4-hydroxyquinoline-3-carboxylic acid
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Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. It plays a key role in constructing the core quinoline structure essential for antibacterial activity. Its functional groups allow for selective modifications, enabling the development of compounds with enhanced potency, solubility, and pharmacokinetic properties. Also investigated for its potential in metal chelation and as a building block in medicinal chemist

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone-class antimicrobial agents. It plays a key role in constructing the core quinoline structure essential for antibacterial activity. Its functional groups allow for selective modifications, enabling the development of compounds with enhanced potency, solubility, and pharmacokinetic properties. Also investigated for its potential in metal chelation and as a building block in medicinal chemistry research targeting enzyme inhibitors.

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