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Structure of 4857-04-9
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2-(Chloromethyl)-1H-benzo[d]imidazole features a reactive chloromethyl handle attached to a rigid, electron-rich benzimidazole core. This combination enables efficient conjugation in synthetic transformations, particularly in the construction of bioconjugates and functionalized heterocycles under mild conditions. The moiety demonstrates stability during handling and compatibility with diverse reaction environments.
2-(Chloromethyl)-1H-benzo[d]imidazole serves as a versatile bifunctional building block, enabling efficient incorporation of both imidazole and chloromethyl moieties into complex architectures. Its reactive chloromethyl group facilitates nucleophilic substitution under mild conditions, while the electron-rich imidazole ring enhances solubility and provides a handle for further derivatization. The compound exhibits excellent bench stability and compatibility with diverse functional groups, making it ideal for modular synthesis of bioactive heterocycles and pharmaceutical intermediates.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: