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Structure of 1205-58-9
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4-(Acetamidomethyl)benzoic acid features a para-substituted benzoic acid core with a strategically positioned acetamidomethyl group, enabling direct conjugation or derivatization in synthetic and bioconjugation workflows. The carboxylic acid moiety offers robust reactivity for amide bond formation, while the acetamido handle provides enhanced solubility and metabolic stability compared to simpler alkyl derivatives. This scaffold integrates seamlessly into peptide and small-molecule design, particularly in targeted delivery systems where controlled hydrophilicity and site-specific attachment are critical.
4-(Acetamidomethyl)benzoic acid serves as a versatile building block for medicinal chemistry and materials science, enabling efficient incorporation of both carboxylic acid and acetamide functionalities in a single scaffold. Its stability under standard reaction conditions facilitates straightforward derivatization, including amide coupling, esterification, and metal-catalyzed transformations, making it well-suited for peptide conjugation, heterocycle synthesis, and API intermediate development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: