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Structure of 857070-66-7
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This bench-stable benzimidazole derivative features a chlorinated aromatic ring and a primary alcohol handle, enabling straightforward derivatization. The para-chloro substitution enhances electrophilicity for cross-coupling reactions, while the hydroxyl group provides polarity and synthetic versatility in pharmaceutical and materials applications.
(2-chloro-1H-benzo[d]imidazol-6-yl)methanol serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient functionalization at the benzoimidazole scaffold. The pendant aldehyde functionality facilitates nucleophilic additions, reductive amination, and coupling reactions under standard conditions. Its bench-stable nature and compatibility with diverse reaction environments make it suitable for iterative synthesis workflows in medicinal chemistry and process development.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: