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Structure of 20033-99-2
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This bench-stable benzimidazole derivative features a methoxy group at the 6-position and a primary alcohol at the 2-position, enabling direct functionalization in synthetic workflows. The electron-rich aromatic core supports efficient coupling reactions, while the hydroxymethyl moiety offers versatility in conjugation strategies.
(6-Methoxy-1H-benzo[d]imidazol-2-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient functionalization at the benzoimidazole C2 position. Its aldehyde functionality facilitates reductive amination, coupling reactions, and conjugation with nucleophiles, while the methoxy group enhances solubility and modulates electronic properties. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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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 : H318
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Precautionary Statements : P280-P305+P351+P338-P310
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Lot numbers can be found on the outside label of a product: