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Structure of 22693-41-0
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2,4,6-Triisopropylbenzenethiol features a sterically shielded aromatic core that enhances stability and resistance to oxidation. The thiol group enables reliable coupling in cross-coupling reactions and surface functionalization. This bench-stable reagent integrates seamlessly into synthetic workflows requiring robust, moisture-tolerant sulfur handles.
2,4,6-Triisopropylbenzenethiol serves as a sterically encumbered thiophenol derivative that facilitates selective thiol-based conjugations and acts as a robust ligand in transition metal catalysis. Its bulky triisopropyl substituents confer enhanced stability and minimize unwanted side reactions, enabling reliable use in functional group interconversions and heterocycle synthesis. The compound exhibits excellent bench stability and simplifies purification in complex reaction mixtures.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H227-H302+H312+H332-H314
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Precautionary Statements : P210-P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: