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Structure of 26798-33-4
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(4-Nitrophenyl)methanethiol features a nitro-substituted phenyl ring linked to a thiol group, combining strong electron-withdrawing character with reactive sulfur functionality. This structure enables efficient conjugation in bioconjugation workflows and facilitates the synthesis of thioether-linked compounds under mild conditions. The molecule exhibits enhanced solubility in organic solvents and stability during storage.
(4-Nitrophenyl)methanethiol serves as a versatile building block for thioether synthesis, enabling efficient conjugation with electrophiles under mild conditions. Its nitro-activated arylthiol functionality offers enhanced reactivity in nucleophilic substitution and metal-catalyzed coupling reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for applications in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3335
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335-H410
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Precautionary Statements : P261-P264-P271-P273-P280-P302+P352-P304+P340-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: