Ethyl 8-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate

98%

Reagent Code: #184471
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CAS Number 31602-18-3

science Other reagents with same CAS 31602-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.24 g/mol
Formula C₁₃H₁₂F₃NO₂
badge Registry Numbers
MDL Number MFCD25542358
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of fluoroquinolone antibiotics, this compound plays a key role in pharmaceutical development due to the presence of the trifluoromethyl group, which enhances metabolic stability and bioavailability. Its structure supports the formation of core quinolone scaffolds important for antimicrobial activity. It is primarily employed in research settings for developing new agents against bacterial infections, especially those involving resistant strains. Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates targeting DNA gyrase and topoisomerase IV.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿15,730.00
250mg
10-20 days ฿25,150.00
Ethyl 8-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate
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Used as an intermediate in the synthesis of fluoroquinolone antibiotics, this compound plays a key role in pharmaceutical development due to the presence of the trifluoromethyl group, which enhances metabolic stability and bioavailability. Its structure supports the formation of core quinolone scaffolds important for antimicrobial activity. It is primarily employed in research settings for developing new agents against bacterial infections, especially those involving resistant strains. Additionally, it s

Used as an intermediate in the synthesis of fluoroquinolone antibiotics, this compound plays a key role in pharmaceutical development due to the presence of the trifluoromethyl group, which enhances metabolic stability and bioavailability. Its structure supports the formation of core quinolone scaffolds important for antimicrobial activity. It is primarily employed in research settings for developing new agents against bacterial infections, especially those involving resistant strains. Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates targeting DNA gyrase and topoisomerase IV.

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