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Structure of 606-18-8
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2-Amino-3-nitrobenzoic acid features a strategically positioned amino group and electron-deficient nitro moiety on the aromatic ring, enabling precise tuning of reactivity in coupling reactions. This ortho-substituted scaffold facilitates efficient integration into bioconjugation workflows and serves as a key intermediate for pharmaceutical and agrochemical synthesis under standard conditions.
2-Amino-3-nitrobenzoic acid serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling the construction of biologically relevant scaffolds through directed functionalization. Its ortho-disubstituted aromatic core provides predictable regiochemistry in coupling and cyclization reactions. The carboxylic acid group facilitates salt formation and derivatization, while the amino and nitro functionalities offer complementary reactivity for sequential transformations. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows requiring controlled redox and coupling sequences.
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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: