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Structure of 13049-16-6
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2-Chloroisophthalic acid features a chlorinated aromatic ring with two carboxylic acid groups in the meta configuration, enabling selective functionalization in polymer synthesis and medicinal chemistry. This bench-stable, moisture-tolerant diacid integrates readily into condensation reactions under standard conditions, offering enhanced solubility and reactivity compared to unsubstituted isophthalic acid derivatives.
2-Chloroisophthalic acid serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized aromatic scaffolds through standard carboxylic acid transformations. Its ortho-chloro and dicarboxylic acid functionalities provide orthogonal reactivity for coupling reactions, derivatization, and heterocycle formation. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in medicinal chemistry and materials science applications.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: