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Structure of 619-73-8
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4-Nitrobenzyl alcohol features a para-nitro group conjugated to a benzylic alcohol, enabling direct functionalization in synthetic workflows. This electron-deficient aromatic scaffold enhances reactivity in nucleophilic substitutions and serves as a robust photolabile protecting group. The hydroxymethyl moiety facilitates derivatization without requiring additional activation steps. Bench-stable under standard conditions, it integrates seamlessly into complex molecule assembly.
4-Nitrobenzyl alcohol serves as a versatile building block in synthetic organic chemistry, enabling efficient introduction of both nitro and hydroxymethyl functionalities. Its bench-stable nature and compatibility with standard protecting group strategies facilitate use in multi-step syntheses. The molecule functions as a key intermediate for heterocycle construction, photochemically cleavable linkers, and functionalized aryl scaffolds relevant to medicinal chemistry and materials science.
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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: