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Structure of 20876-30-6
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This acetic acid derivative features a methoxy-substituted nitroaryl group, offering enhanced solubility and stability in organic synthesis. The para-nitro functionality enables efficient coupling reactions, while the ortho-methoxy substituent modulates electronic properties. Ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
2-(4-Methoxy-2-nitrophenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of nitro-substituted aryl acetic acid derivatives. Its ortho-nitro and para-methoxy groups provide complementary electronic modulation and enhance reactivity in coupling and reduction processes. The carboxylic acid functionality facilitates straightforward derivatization, while the molecule exhibits good bench stability and ease of purification—key attributes for scalable synthetic workflows.
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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: