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Structure of 6758-34-5
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This trifluoromethyl-substituted benzimidazole derivative features a reactive hydroxymethyl group enabling direct functionalization. The electron-deficient benzimidazole core enhances stability and modulates electronic properties, while the trifluoromethyl moiety imparts strong lipophilicity and metabolic resistance. Ideal for bioconjugation and pharmaceutical intermediates.
(6-(Trifluoromethyl)-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 stable trifluoromethyl group enhances metabolic resistance and lipophilicity, while the primary alcohol facilitates derivatization via esterification, ether formation, or oxidation to aldehyde. The compound exhibits excellent bench stability and compatibility with standard coupling conditions, making it suitable for medicinal chemistry campaigns requiring targeted scaffold elaboration.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: