Methyl 3-ethynyl-4-fluorobenzoate

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Reagent Code: #65091
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CAS Number 1263286-05-0

science Other reagents with same CAS 1263286-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.16 g/mol
Formula C₁₀H₇FO₂
badge Registry Numbers
MDL Number MFCD17676553
thermostat Physical Properties
Boiling Point 253.3±30.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both an ethynyl group and a fluorine atom on a benzoate backbone, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The ethynyl group allows for further functionalization through reactions like Sonogashira coupling, enabling the creation of diverse compounds. Additionally, the presence of the fluorine atom can enhance the biological activity and stability of the resulting molecules, making it a useful component in drug discovery and development. Its application is also seen in materials science, where it contributes to the synthesis of specialized polymers and advanced materials with unique properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,647.00

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Methyl 3-ethynyl-4-fluorobenzoate
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both an ethynyl group and a fluorine atom on a benzoate backbone, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The ethynyl group allows for further functionalization through reactions like Sonogashira coupling, enabling the creation of diverse compounds. Additionally, the presence of th

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both an ethynyl group and a fluorine atom on a benzoate backbone, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The ethynyl group allows for further functionalization through reactions like Sonogashira coupling, enabling the creation of diverse compounds. Additionally, the presence of the fluorine atom can enhance the biological activity and stability of the resulting molecules, making it a useful component in drug discovery and development. Its application is also seen in materials science, where it contributes to the synthesis of specialized polymers and advanced materials with unique properties.

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