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Structure of 106131-61-7
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3,6-Dichloro-1,2,4,5-tetrazine features a highly reactive tetrazine core with two chlorine substituents at the 3 and 6 positions, enabling efficient inverse electron-demand Diels-Alder reactions. This bench-stable compound integrates readily into bioorthogonal labeling workflows, offering rapid conjugation kinetics with strained dienophiles. The electron-deficient framework enhances selectivity in complex biological environments.
3,6-Dichloro-1,2,4,5-tetrazine serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of nitrogen-rich heterocycles and functionalized scaffolds. Its reactive dichloro substituents facilitate selective nucleophilic substitution under mild conditions, offering high functional group tolerance and compatibility with common coupling protocols. The compound exhibits excellent bench stability and simplifies purification in multi-step syntheses, making it well-suited for the development of advanced intermediates in medicinal chemistry and materials science applications.
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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: