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Structure of 331949-55-4
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This bench-stable benzimidazole derivative features a chlorinated aromatic core and a primary alcohol handle, enabling straightforward functionalization. The methyl group enhances solubility, while the chloro substituent provides a site for cross-coupling reactions. This scaffold serves as a building block in medicinal chemistry and materials synthesis.
(6-Chloro-1-methyl-1H-benzo[d]imidazol-2-yl)methanol serves as a versatile building block for bioactive heterocycles, enabling direct functionalization at the benzoimidazole C2 position. Its pendant alcohol group facilitates derivatization via esterification, etherification, or oxidation to aldehyde, while the 6-chloro and 1-methyl substituents provide orthogonal reactivity for cross-coupling or nucleophilic substitution. Bench-stable and compatible with standard purification methods, it supports efficient synthesis of pharmaceutical intermediates and functionalized scaffolds in medicinal chemistry workflows.
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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-H332-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: