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Structure of 92972-48-0
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2,4-Dichloro-5-thiazolecarboxaldehyde features a reactive aldehyde group flanked by electron-withdrawing chlorine substituents and a thiazole ring, delivering enhanced electrophilicity for targeted conjugation. This bench-stable scaffold integrates readily into heterocyclic architectures, enabling efficient synthesis of bioactive intermediates in medicinal chemistry and agrochemical development.
2,4-Dichloro-5-thiazolecarboxaldehyde serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the thiazole ring for medicinal chemistry and agrochemical development. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the dichloro substituents provide orthogonal reactivity for further derivatization. The compound exhibits good bench stability and is compatible with standard purification techniques, making it suitable for scale-up and multi-step synthesis workflows.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: