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Structure of 464152-38-3
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This acetic acid derivative features a methoxypyridine moiety that enhances solubility and metabolic stability. It serves as a key scaffold in bioactive molecule design, particularly in kinase inhibitors and pharmaceutical intermediates. The para-methoxy group provides electron-donating character, while the carboxylic acid enables facile derivatization.
2-(2-Methoxypyridin-4-yl)acetic acid serves as a versatile building block for constructing bioactive heterocycles and pharmaceutical intermediates. Its pyridine core enables metal-catalyzed cross-coupling, while the carboxylic acid group facilitates amide bond formation and derivatization. The methoxy substituent enhances solubility and modulates electronic properties, contributing to improved stability and ease of purification in 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: