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Structure of 130551-92-7
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Oxazol-2-ylmethanol delivers a reactive hydroxymethyl handle attached to a heteroaromatic oxazole ring. This bench-stable scaffold integrates readily into synthetic sequences, enabling direct functionalization at the benzylic position. The molecule features high solubility in common organic solvents and exhibits robust stability under standard reaction conditions. Its polar yet aromatic character supports diverse applications in medicinal chemistry and materials synthesis.
Oxazol-2-ylmethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to oxazole-containing scaffolds through standard functional group transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward derivatization, including oxidation to the carboxylic acid or substitution at the hydroxymethyl position. This compound functions effectively in coupling reactions and heterocycle elaboration, supporting reliable synthesis of bioactive molecules and API intermediates.
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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: