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Structure of 77376-03-5
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This amino-nitrobenzyl alcohol integrates a reactive hydroxymethyl group with an electron-deficient aromatic core, enabling straightforward conjugation and functionalization. The para-substituted scaffold supports efficient derivatization under mild conditions, making it valuable for bioconjugation and probe synthesis.
(5-Amino-2-nitrophenyl)methanol serves as a versatile building block for heterocyclic synthesis and functionalized aromatic systems. The molecule combines an amino group ortho to a nitro function with a benzylic alcohol, enabling sequential transformations such as reduction, coupling, or cyclization. Its bench-stable nature and compatibility with standard protecting group strategies facilitate reliable use in multi-step synthetic sequences for medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: