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Structure of 51307-43-8
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This (2-Aminothiazol-4-yl)methanol features a reactive amino-thiazole scaffold paired with a primary alcohol, enabling direct conjugation or derivatization in synthetic workflows. The molecule integrates readily into bioconjugation strategies and serves as a key intermediate for heterocyclic compound libraries.
(2-Aminothiazol-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based scaffolds through straightforward functionalization. Its primary amine and hydroxymethyl groups offer orthogonal reactivity for conjugation, derivatization, and coupling reactions. The compound exhibits good bench stability and facilitates purification via standard chromatographic methods, making it well-suited for iterative synthesis workflows in API development and target-oriented discovery.
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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: