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Structure of 4887-94-9
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2-Chloro-5-methyl-1H-benzo[d]imidazole features a fused bicyclic core with complementary electron-withdrawing and electron-donating substituents, enabling robust coupling reactions in synthetic medicinal chemistry. This bench-stable heterocycle integrates readily into bioactive scaffolds requiring halogen-directed functionalization.
2-Chloro-5-methyl-1H-benzo[d]imidazole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of bioactive scaffolds. Its electrophilic chlorine and electron-rich aromatic system facilitate palladium-catalyzed cross-coupling reactions, while the methyl group provides a handle for further functionalization. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H317-H319-H410
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Precautionary Statements : P261-P264-P272-P273-P280-P302+P352-P362-P391-P501
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Lot numbers can be found on the outside label of a product: