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Structure of 51-39-8
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3,4,5-Trichlorobenzoic acid features a highly electron-deficient aromatic ring stabilized by three chlorine substituents. This configuration enhances its utility in electrophilic substitution reactions and as a building block for functionalized heterocycles. The compound exhibits excellent bench stability and solubility in common organic solvents, facilitating straightforward handling in synthetic workflows.
3,4,5-Trichlorobenzoic acid serves as a robust building block in medicinal chemistry and agrochemical synthesis, offering high functional group tolerance and excellent bench stability. Its three chlorine substituents enhance electrophilic reactivity and facilitate downstream derivatization via amide formation, esterification, or coupling reactions. The compound functions effectively in standard peptide coupling protocols and enables efficient access to chlorinated aromatic scaffolds relevant to API 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-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: