Ethyl 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylate

95%

Reagent Code: #183489
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CAS Number 105404-65-7

science Other reagents with same CAS 105404-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.40 g/mol
Formula C₁₉H₂₂FN₃O₃
badge Registry Numbers
MDL Number MFCD24038928
thermostat Physical Properties
Boiling Point 555.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Widely used as an intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of ciprofloxacin and related antimicrobial agents. Its structure allows for key modifications that enhance antibacterial activity, especially against Gram-negative and some Gram-positive bacteria. The compound plays a critical role in pharmaceutical manufacturing due to its ability to form active pharmacophores when further functionalized. It is commonly employed in batch processes to ensure high yield and purity of the final drug substance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,100.00
inventory 1g
10-20 days ฿15,810.00
inventory 5g
10-20 days ฿57,590.00
inventory 250mg
10-20 days ฿5,280.00
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Ethyl 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylate
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Widely used as an intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of ciprofloxacin and related antimicrobial agents. Its structure allows for key modifications that enhance antibacterial activity, especially against Gram-negative and some Gram-positive bacteria. The compound plays a critical role in pharmaceutical manufacturing due to its ability to form active pharmacophores when further functionalized. It is commonly employed in batch processes to ensure hig

Widely used as an intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of ciprofloxacin and related antimicrobial agents. Its structure allows for key modifications that enhance antibacterial activity, especially against Gram-negative and some Gram-positive bacteria. The compound plays a critical role in pharmaceutical manufacturing due to its ability to form active pharmacophores when further functionalized. It is commonly employed in batch processes to ensure high yield and purity of the final drug substance.

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