Diphenyliodonium trifluoromethanesulfonate
98%
Reagent
Code: #122107
Alias
Diphenyliodotrifluoromethanesulfonate
CAS Number
66003-76-7
blur_circular Chemical Specifications
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Molecular Information
Weight
430.18 g/mol
Formula
C₁₃H₁₀F₃IO₃S
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Registry Numbers
MDL Number
MFCD00191356
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Physical Properties
Melting Point
46-49 °C(lit.)
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Storage & Handling
Storage
room temperature, away from light
description Product Description
Diphenyliodonium trifluoromethanesulfonate is widely used as a photoacid generator in photoresist formulations for the semiconductor industry. It plays a critical role in the photolithography process, where it generates strong acids upon exposure to UV light, facilitating the patterning of microelectronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in cationic polymerization reactions, where it acts as an efficient initiator. Its strong oxidizing properties also make it useful in various organic transformations, including cross-coupling reactions and the functionalization of aromatic compounds. In advanced materials science, it is utilized to modify surfaces and create thin films with specific properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (Ion Exchange Titration) | 97.5-102.5 |
Melting Point | 177-183 |
Solubility in Methanol | Almost transparent |
Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
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Diphenyliodonium trifluoromethanesulfonate
Diphenyliodonium trifluoromethanesulfonate is widely used as a photoacid generator in photoresist formulations for the semiconductor industry. It plays a critical role in the photolithography process, where it generates strong acids upon exposure to UV light, facilitating the patterning of microelectronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in cationic polymerization reactions, where it acts as an efficient initiator. Its strong oxidizing properties also make it useful in various organic transformations, including cross-coupling reactions and the functionalization of aromatic compounds. In advanced materials science, it is utilized to modify surfaces and create thin films with specific properties.
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