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Structure of 39070-14-9
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This bench-stable imidazole derivative features a nitro group at the 2-position and a methanol side chain at C1, enabling direct functionalization in synthetic workflows. The electron-deficient heterocycle pairs effectively with nucleophiles, while the hydroxyl moiety offers a handle for derivatization.
(1-Methyl-2-nitro-1H-imidazol-5-yl)methanol serves as a versatile building block for nitro-imidazole derivatives, enabling efficient access to heterocyclic scaffolds relevant in medicinal chemistry. Its benzylic alcohol functionality facilitates oxidation, protection, or coupling reactions, while the electron-deficient imidazole ring supports nucleophilic substitution and metal-catalyzed transformations. The compound exhibits good bench stability and compatibility with standard synthetic protocols, making it suitable for modular library synthesis and API intermediate 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: