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Structure of 933683-87-5
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2-Ethylthiazole-5-carbaldehyde features a thiazole ring bearing an ethyl substituent at the 2-position and a formyl group at the 5-position, delivering a potent electrophilic handle. This scaffold integrates readily into heterocyclic synthesis, offering enhanced solubility and stability compared to analogs. The aldehyde functionality enables efficient coupling reactions in medicinal chemistry and materials science applications.
2-Ethylthiazole-5-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient construction of thiazole-based pharmacophores. Its aldehyde functionality facilitates reductive amination, Grignard additions, and condensation reactions with amines or hydrazines under standard conditions. The ethyl substituent enhances solubility and modulates electronic properties without compromising bench stability. This compound functions reliably in multistep syntheses requiring orthogonal functional group compatibility and offers straightforward purification via crystallization or flash chromatography.
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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-P363
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Lot numbers can be found on the outside label of a product: