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Structure of 136663-40-6
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This bench-stable benzoxazole derivative integrates a reactive benzylic alcohol group, enabling straightforward functionalization in synthetic workflows. The electron-rich aromatic system enhances compatibility with transition-metal-catalyzed couplings, while the methyl substitution improves solubility and stability under standard conditions.
(2-Methyl-1,3-benzoxazol-6-yl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the benzylic position. Its benzoxazole core provides enhanced metabolic stability and favorable pharmacokinetic properties, while the primary alcohol facilitates straightforward derivatization via oxidation, esterification, or coupling reactions. The molecule exhibits good bench stability and compatibility with standard synthetic protocols, making it well-suited for use in the construction of bioactive heterocycles 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: