p-Tolyl Trifluoromethanesulfonate

98%

Reagent Code: #121844
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CAS Number 29540-83-8

science Other reagents with same CAS 29540-83-8

blur_circular Chemical Specifications

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Weight 240.2 g/mol
Formula C₈H₇F₃O₃S
badge Registry Numbers
MDL Number MFCD00192507
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description Product Description

p-Tolyl Trifluoromethanesulfonate (4-methylphenyl triflate) is a valuable intermediate in organic synthesis, particularly for the formation of carbon-carbon bonds. It functions as an electrophile in palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura, Heck, and Sonogashira couplings, where the triflate serves as an excellent leaving group, often outperforming aryl halides. This compound is also utilized in other metal-mediated transformations to introduce aryl groups into complex molecules. Its stability and reactivity make it essential in the production of pharmaceuticals, agrochemicals, and advanced materials.

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Test Parameter Specification
Appearance Colorless To Light Yellow Liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,270.00
inventory 5g
10-20 days ฿5,650.00

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p-Tolyl Trifluoromethanesulfonate
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p-Tolyl Trifluoromethanesulfonate (4-methylphenyl triflate) is a valuable intermediate in organic synthesis, particularly for the formation of carbon-carbon bonds. It functions as an electrophile in palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura, Heck, and Sonogashira couplings, where the triflate serves as an excellent leaving group, often outperforming aryl halides. This compound is also utilized in other metal-mediated transformations to introduce aryl groups into complex molec

p-Tolyl Trifluoromethanesulfonate (4-methylphenyl triflate) is a valuable intermediate in organic synthesis, particularly for the formation of carbon-carbon bonds. It functions as an electrophile in palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura, Heck, and Sonogashira couplings, where the triflate serves as an excellent leaving group, often outperforming aryl halides. This compound is also utilized in other metal-mediated transformations to introduce aryl groups into complex molecules. Its stability and reactivity make it essential in the production of pharmaceuticals, agrochemicals, and advanced materials.

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