Ethyl 7-Chloro-4-Hydroxy-8-Methylquinoline-3-Carboxylate

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Reagent Code: #51251
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CAS Number 5350-94-7

science Other reagents with same CAS 5350-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.7 g/mol
Formula C₁₃H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD00173377
thermostat Physical Properties
Boiling Point 395.6 °C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is crucial for developing medications with antibacterial and antimalarial properties. Additionally, it finds application in organic synthesis, where it acts as a building block for more complex molecules. Researchers also utilize it in the study of chemical reactions involving heterocyclic compounds, aiding in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿60,291.00
inventory 250mg
10-20 days ฿7,191.00
inventory 1g
10-20 days ฿17,091.00

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Ethyl 7-Chloro-4-Hydroxy-8-Methylquinoline-3-Carboxylate
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Used primarily in the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is crucial for developing medications with antibacterial and antimalarial properties. Additionally, it finds application in organic synthesis, where it acts as a building block for more complex molecules. Researchers also utilize it in the study of chemical reactions involving heterocyclic compounds, aiding in the discovery of new therapeutic agents.

Used primarily in the pharmaceutical industry, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is crucial for developing medications with antibacterial and antimalarial properties. Additionally, it finds application in organic synthesis, where it acts as a building block for more complex molecules. Researchers also utilize it in the study of chemical reactions involving heterocyclic compounds, aiding in the discovery of new therapeutic agents.

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