3-Methylisoxazol-5-yl trifluoromethanesulfonate

95%

Reagent Code: #87380
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CAS Number 1363210-15-4

science Other reagents with same CAS 1363210-15-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.15 g/mol
Formula C₅H₄F₃NO₄S
badge Registry Numbers
MDL Number MFCD23378510
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound, 3-Methylisoxazol-5-yl trifluoromethanesulfonate, is a versatile reagent in organic synthesis, particularly for building complex molecules incorporating the isoxazole scaffold. It acts as an electrophile in cross-coupling reactions, such as Suzuki and Heck couplings, where the trifluoromethanesulfonate group serves as an excellent leaving group to enable the formation of carbon-carbon and carbon-heteroatom bonds. This functionality is essential for synthesizing intermediates used in pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity also make it suitable for developing biologically active compounds and heterocycles critical to drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,445.00
inventory 250mg
10-20 days ฿26,622.00

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3-Methylisoxazol-5-yl trifluoromethanesulfonate
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This compound, 3-Methylisoxazol-5-yl trifluoromethanesulfonate, is a versatile reagent in organic synthesis, particularly for building complex molecules incorporating the isoxazole scaffold. It acts as an electrophile in cross-coupling reactions, such as Suzuki and Heck couplings, where the trifluoromethanesulfonate group serves as an excellent leaving group to enable the formation of carbon-carbon and carbon-heteroatom bonds. This functionality is essential for synthesizing intermediates used in pharmac

This compound, 3-Methylisoxazol-5-yl trifluoromethanesulfonate, is a versatile reagent in organic synthesis, particularly for building complex molecules incorporating the isoxazole scaffold. It acts as an electrophile in cross-coupling reactions, such as Suzuki and Heck couplings, where the trifluoromethanesulfonate group serves as an excellent leaving group to enable the formation of carbon-carbon and carbon-heteroatom bonds. This functionality is essential for synthesizing intermediates used in pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity also make it suitable for developing biologically active compounds and heterocycles critical to drug discovery and development.

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