1,1,1,3,3,3-Hexafluoroisopropyl p-Toluenesulfonate

≥98%(GC)

Reagent Code: #57753
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CAS Number 67674-48-0

science Other reagents with same CAS 67674-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.22 g/mol
Formula C₁₀H₈F₆O₃S
badge Registry Numbers
MDL Number MFCD00039262
thermostat Physical Properties
Melting Point 45°C
Boiling Point 134°C|22.5mmHg(lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used as a reagent in organic synthesis, particularly in the preparation of fluorinated compounds. It serves as a versatile fluorinating agent, enabling the introduction of hexafluoroisopropyl groups into various organic molecules. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials, where fluorinated compounds often exhibit enhanced stability, bioavailability, and unique properties. Additionally, it is employed in the synthesis of specialty polymers and coatings, contributing to improved performance characteristics such as chemical resistance and thermal stability. Its role in facilitating complex chemical transformations makes it valuable in research and industrial processes.

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inventory 5g
10-20 days ฿1,800.00

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1,1,1,3,3,3-Hexafluoroisopropyl p-Toluenesulfonate
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This chemical is primarily used as a reagent in organic synthesis, particularly in the preparation of fluorinated compounds. It serves as a versatile fluorinating agent, enabling the introduction of hexafluoroisopropyl groups into various organic molecules. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials, where fluorinated compounds often exhibit enhanced stability, bioavailability, and unique properties. Additionally, it is employed in the synt

This chemical is primarily used as a reagent in organic synthesis, particularly in the preparation of fluorinated compounds. It serves as a versatile fluorinating agent, enabling the introduction of hexafluoroisopropyl groups into various organic molecules. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials, where fluorinated compounds often exhibit enhanced stability, bioavailability, and unique properties. Additionally, it is employed in the synthesis of specialty polymers and coatings, contributing to improved performance characteristics such as chemical resistance and thermal stability. Its role in facilitating complex chemical transformations makes it valuable in research and industrial processes.

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