Phenyl p-Toluenesulfonate

99%,GC

Reagent Code: #225473
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CAS Number 640-60-8

science Other reagents with same CAS 640-60-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.3 g/mol
Formula C₁₃H₁₂O₃S
badge Registry Numbers
MDL Number MFCD00025996
thermostat Physical Properties
Melting Point 94-98°C
Boiling Point 385.8°C
inventory_2 Storage & Handling
Density 1.245g/cm3
Storage Room temperature, inert gas environment

description Product Description

Phenyl p-toluenesulfonate is an aryl sulfonate ester primarily employed in organic synthesis as an electrophile in transition-metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura, Sonogashira, and Buchwald-Hartwig couplings, where the tosylate group functions as a leaving group for forming C-C, C-O, and C-N bonds. Its stability and selectivity make it suitable for preparing intermediates in pharmaceuticals, agrochemicals, and fine chemicals. It is also used in the synthesis of aryl-substituted dyes and specialty polymers requiring controlled arylation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿1,850.00
inventory 25g
10-20 days ฿5,150.00
inventory 100g
10-20 days ฿13,040.00
Phenyl p-Toluenesulfonate
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Phenyl p-toluenesulfonate is an aryl sulfonate ester primarily employed in organic synthesis as an electrophile in transition-metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura, Sonogashira, and Buchwald-Hartwig couplings, where the tosylate group functions as a leaving group for forming C-C, C-O, and C-N bonds. Its stability and selectivity make it suitable for preparing intermediates in pharmaceuticals, agrochemicals, and fine chemicals. It is also used in the synthesis of aryl-substituted d
Phenyl p-toluenesulfonate is an aryl sulfonate ester primarily employed in organic synthesis as an electrophile in transition-metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura, Sonogashira, and Buchwald-Hartwig couplings, where the tosylate group functions as a leaving group for forming C-C, C-O, and C-N bonds. Its stability and selectivity make it suitable for preparing intermediates in pharmaceuticals, agrochemicals, and fine chemicals. It is also used in the synthesis of aryl-substituted dyes and specialty polymers requiring controlled arylation.
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