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Structure of 5683-43-2
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2-Methyl-6-nitrobenzoxazole features a fused heterocyclic core with complementary electron-withdrawing and steric influences. The para-nitro group enhances electrophilicity, while the methyl substituent provides modest steric shielding. This combination enables reliable participation in cross-coupling reactions and facilitates incorporation into advanced photonic materials and bioactive scaffolds under standard conditions.
2-Methyl-6-nitrobenzoxazole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to biologically active scaffolds. Its electron-deficient aromatic core facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions. The methyl and nitro groups provide orthogonal handles for selective functionalization, while the benzoxazole framework offers metabolic stability and favorable pharmacokinetic properties. This compound exhibits excellent bench stability and is compatible with standard purification methods, making it ideal for iterative synthesis workflows in drug discovery and process development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318
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Precautionary Statements : P264-P270-P280-P305+P351+P338-P330-P501
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Lot numbers can be found on the outside label of a product: