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Structure of 18672-03-2
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5,6-Dichloro-1H-benzo[d]imidazol-2-amine features two chlorine atoms at the 5 and 6 positions of the imidazole ring, enhancing electron deficiency and reactivity. This bench-stable heterocycle serves as a key scaffold in medicinal chemistry for kinase inhibitors and bioactive compound synthesis.
5,6-Dichloro-1H-benzo[d]imidazol-2-amine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. The molecule exhibits robust bench stability and facilitates efficient functionalization at the imidazole nitrogen, enabling straightforward incorporation into diverse scaffolds. Its dual chloro substituents enhance electrophilic reactivity in cross-coupling reactions and support downstream derivatization via palladium-catalyzed transformations. This compound functions as a key intermediate in the synthesis of bioactive molecules and advanced functional materials.
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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: