5-Fluoroquinoline-8-carboxylic acid

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Reagent Code: #131884
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CAS Number 926252-31-5

science Other reagents with same CAS 926252-31-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.16 g/mol
Formula C₁₀H₆FNO₂
badge Registry Numbers
MDL Number MFCD09048900
thermostat Physical Properties
Boiling Point 388.9±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.431±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, enhancing antimicrobial activity against a broad spectrum of bacteria. Its structure supports the development of drugs targeting DNA gyrase and topoisomerase IV, critical for bacterial replication. Also explored in medicinal chemistry for anticancer and antiviral research due to its ability to intercalate with nucleic acids and modulate enzyme activity. Commonly employed in the preparation of complex heterocyclic compounds for pharmaceutical development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,820.00
inventory 250mg
10-20 days ฿11,580.00
inventory 1g
10-20 days ฿31,220.00

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5-Fluoroquinoline-8-carboxylic acid
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Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, enhancing antimicrobial activity against a broad spectrum of bacteria. Its structure supports the development of drugs targeting DNA gyrase and topoisomerase IV, critical for bacterial replication. Also explored in medicinal chemistry for anticancer and antiviral research due to its ability to intercalate with nucleic acids and modulate enzyme activity. Commonly employed in the preparation of complex heterocyclic compounds for ph

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, enhancing antimicrobial activity against a broad spectrum of bacteria. Its structure supports the development of drugs targeting DNA gyrase and topoisomerase IV, critical for bacterial replication. Also explored in medicinal chemistry for anticancer and antiviral research due to its ability to intercalate with nucleic acids and modulate enzyme activity. Commonly employed in the preparation of complex heterocyclic compounds for pharmaceutical development.

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