Methyl 4-hydroxyquinoline-2-carboxylate

98%

Reagent Code: #206686
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CAS Number 5965-59-3

science Other reagents with same CAS 5965-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
thermostat Physical Properties
Boiling Point 331.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. It plays a key role in constructing the core quinoline scaffold essential for antimicrobial efficacy. Also employed in research for developing novel bioactive molecules with potential antiviral and anticancer properties. Its functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,000.00
5g
10-20 days ฿4,800.00
10g
10-20 days ฿9,590.00
25g
10-20 days ฿23,950.00
Methyl 4-hydroxyquinoline-2-carboxylate
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Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. It plays a key role in constructing the core quinoline scaffold essential for antimicrobial efficacy. Also employed in research for developing novel bioactive molecules with potential antiviral and anticancer properties. Its functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activ

Used as an intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. It plays a key role in constructing the core quinoline scaffold essential for antimicrobial efficacy. Also employed in research for developing novel bioactive molecules with potential antiviral and anticancer properties. Its functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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