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Structure of 95453-59-1
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2-Methoxythiazole-5-carbaldehyde features a reactive aldehyde group appended to a thiazole scaffold bearing a methoxy substituent. This combination delivers enhanced solubility and stability under standard conditions, enabling direct integration into heterocyclic synthesis workflows. The electron-rich thiazole ring facilitates efficient coupling reactions, while the para-positioned aldehyde serves as a key handle for derivatization in medicinal chemistry and materials development.
2-Methoxythiazole-5-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and process development. Its aldehyde functionality enables direct incorporation into Ugi, Mannich, or reductive amination reactions, while the methoxy group enhances solubility and modulates electronic properties. The thiazole core provides structural rigidity and metabolic stability, making it valuable in the synthesis of kinase inhibitors and other bioactive scaffolds. Bench-stable and compatible with standard protecting group strategies, it facilitates efficient route design and purification.
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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: