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Structure of 139669-95-7
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2,4-Dibromothiazole-5-carbaldehyde features a brominated thiazole core with an aldehyde handle at the 5-position, enabling direct functionalization in cross-coupling and heterocycle construction. The electron-deficient aromatic system enhances reactivity in nucleophilic substitution, while the bench-stable carbonyl group facilitates downstream derivatization under standard conditions.
2,4-Dibromothiazole-5-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the 5-position via nucleophilic substitution or transition-metal-catalyzed coupling. The aldehyde group facilitates efficient derivatization through oxidation, reduction, or condensation reactions, while the bromine substituents offer orthogonal reactivity for cross-coupling protocols. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthesis workflows in medicinal chemistry and materials science.
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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: