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Structure of 65373-53-7
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1,2-Oxazole-4-carbaldehyde features a reactive aldehyde group fused to an electron-deficient oxazole ring, enabling direct coupling in heterocyclic synthesis. This bench-stable scaffold integrates readily into bioactive molecule design, offering high functional group tolerance and efficient access to complex nitrogen-containing architectures under standard conditions.
1,2-Oxazole-4-carbaldehyde serves as a versatile synthon in heterocyclic synthesis, enabling direct functionalization at the C4 position via electrophilic or nucleophilic transformations. Its aldehyde group facilitates imine formation and reductive amination, while the oxazole ring provides stability and orthogonal reactivity. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it a practical building block for medicinal chemistry and API development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: