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Structure of 173998-77-1
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1-N-Boc-2-Methyl-Isothiourea features a protected isothiourea core with a methyl group at the 2-position, offering enhanced stability and controlled reactivity. This bench-stable derivative enables selective incorporation into peptide architectures and functional materials, serving as a reliable scaffold for bioconjugation and medicinal chemistry applications.
1-N-Boc-2-Methyl-Isothiourea serves as a stable, bench-ready isothiourea derivative enabling efficient nucleophilic catalysis in amide bond formation and urea synthesis. Its Boc-protected nitrogen enhances functional group tolerance and simplifies purification, while the methyl substitution improves reactivity in standard coupling protocols. Functions reliably in peptide coupling and heterocycle construction workflows with minimal side-product formation.
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GHS Pictogram :
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: