7,8-Difluoro-2-methylquinolin-3-ol

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Reagent Code: #131348
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CAS Number 1314012-50-4

science Other reagents with same CAS 1314012-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.17 g/mol
Formula C₁₀H₇F₂NO
badge Registry Numbers
MDL Number MFCD27938306
thermostat Physical Properties
Boiling Point 313.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.395±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. It serves in developing kinase inhibitors and antiviral agents due to its ability to enhance binding affinity and metabolic stability. Also applied in the design of fluorescent probes for biochemical imaging, leveraging the electron-withdrawing effects of fluorine atoms to tune optical properties. Its structure supports research in drug discovery targeting oncology and infectious diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,740.00
inventory 250mg
10-20 days ฿25,080.00

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7,8-Difluoro-2-methylquinolin-3-ol
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Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. It serves in developing kinase inhibitors and antiviral agents due to its ability to enhance binding affinity and metabolic stability. Also applied in the design of fluorescent probes for biochemical imaging, leveraging the electron-withdrawing effects of fluorine atoms to tune optical properties. Its structure supports research in drug discovery targeting oncology and

Used as a key intermediate in the synthesis of fluorinated quinoline derivatives, which show biological activity in medicinal chemistry. It serves in developing kinase inhibitors and antiviral agents due to its ability to enhance binding affinity and metabolic stability. Also applied in the design of fluorescent probes for biochemical imaging, leveraging the electron-withdrawing effects of fluorine atoms to tune optical properties. Its structure supports research in drug discovery targeting oncology and infectious diseases.

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