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Structure of 24691-30-3
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This pyrrole carboxylic acid features a sterically hindered, electron-deficient core with dual chlorine substituents at the 3,4-positions and a methyl group at the 5-position. The carboxylic acid functionality enables direct coupling in peptide synthesis or derivatization workflows. Bench-stable under standard conditions, it integrates readily into complex heterocyclic architectures.
3,4-Dichloro-5-methyl-1H-pyrrole-2-carboxylic acid serves as a versatile building block for heterocyclic synthesis, offering defined substitution patterns ideal for medicinal chemistry and agrochemical development. The carboxylic acid functionality enables direct coupling reactions, while the dichloro and methyl groups provide orthogonal reactivity and metabolic stability. Its bench-stable nature and compatibility with standard peptide coupling protocols facilitate efficient incorporation into complex molecular architectures.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: