7-Chloro-4-hydroxyquinoline-3-carboxylic acid

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Reagent Code: #159900
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CAS Number 86-47-5

science Other reagents with same CAS 86-47-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.61 g/mol
Formula C₁₀H₆ClNO₃
badge Registry Numbers
MDL Number MFCD00038080
thermostat Physical Properties
Melting Point 250°C dec. (Lit.)
Boiling Point 416.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolones, which are broad-spectrum antimicrobial agents. It plays a crucial role in forming the core structure of drugs effective against bacterial infections including urinary tract infections, respiratory infections, and certain sexually transmitted diseases. Its functional groups allow for chemical modifications that enhance antibacterial activity and pharmacokinetic properties in final drug compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,090.00
inventory 250mg
10-20 days ฿2,010.00

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7-Chloro-4-hydroxyquinoline-3-carboxylic acid
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Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolones, which are broad-spectrum antimicrobial agents. It plays a crucial role in forming the core structure of drugs effective against bacterial infections including urinary tract infections, respiratory infections, and certain sexually transmitted diseases. Its functional groups allow for chemical modifications that enhance antibacterial activity and pharmacokinetic properties in final drug

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolones, which are broad-spectrum antimicrobial agents. It plays a crucial role in forming the core structure of drugs effective against bacterial infections including urinary tract infections, respiratory infections, and certain sexually transmitted diseases. Its functional groups allow for chemical modifications that enhance antibacterial activity and pharmacokinetic properties in final drug compounds.

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