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Structure of 77189-99-2
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2,4,6-Trimethoxybenzenethiol features a benzene ring substituted with three methoxy groups and a thiol moiety, delivering enhanced solubility and stability. The electron-donating methoxy groups increase the nucleophilicity of the thiol, enabling efficient coupling in synthetic transformations. This bench-stable reagent integrates readily into sulfur-containing compound syntheses.
2,4,6-Trimethoxybenzenethiol serves as a versatile building block in synthetic organic chemistry, offering enhanced solubility and stability compared to unsubstituted thiophenols. Its three methoxy groups provide strong electron-donating effects, facilitating nucleophilic substitution reactions and enabling efficient coupling with electrophilic partners. The molecule functions effectively in the construction of heterocyclic scaffolds and serves as a key intermediate in the synthesis of functionalized aromatic systems for pharmaceutical and agrochemical applications.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302+H312+H332-H315-H319
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: