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Structure of 917828-31-0
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5-Cyclopropyl-1,3-oxazole-4-carboxylic acid features a rigid oxazole core with a cyclopropyl substituent at the 5-position, enhancing lipophilicity and metabolic stability. The carboxylic acid group enables direct conjugation or derivatization in medicinal chemistry campaigns. This scaffold integrates readily into bioactive molecules requiring moderate polarity and structural rigidity under standard bench conditions.
5-Cyclopropyl-1,3-oxazole-4-carboxylic acid serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to oxazole-based scaffolds. Its cyclopropyl substituent enhances metabolic stability and modulates lipophilicity, while the carboxylic acid group facilitates direct coupling reactions or derivatization. The compound exhibits bench stability and compatibility with standard synthetic protocols, making it well-suited for iterative library synthesis 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: