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Structure of 13452-14-7
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2-Methyl-1,3-benzoxazole-6-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 6-position, enabling direct conjugation in synthetic workflows. The methyl substituent enhances electronic density at the aromatic ring, while the oxazole scaffold imparts stability and planarity. This compound serves as a key building block for bioactive molecule synthesis, particularly in medicinal chemistry and materials science applications.
2-Methyl-1,3-benzoxazole-6-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through standard coupling and functionalization reactions. Its carboxylic acid group facilitates direct amide formation and derivatization, while the benzoxazole core provides structural rigidity and metabolic stability. Bench-stable and compatible with common reaction conditions, it supports scalable synthesis in medicinal chemistry and materials applications.
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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-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: