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Structure of 636-69-1
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2-Hydroxyheptanoic acid features a hydroxyl group at the alpha position relative to the carboxylic acid, enhancing its polarity and reactivity in esterification and coupling reactions. This configuration supports its use in chiral synthesis and as a building block for bioactive molecules. The molecule exhibits favorable solubility in polar organic solvents and stability under standard bench conditions.
2-Hydroxyheptanoic acid serves as a versatile chiral building block in synthetic organic chemistry, enabling access to diverse functionalized intermediates. Its α-hydroxy carboxylic acid structure facilitates stereoselective transformations, including aldol reactions and cyclizations, while offering moderate bench stability and straightforward purification via crystallization or extraction. Functions effectively in the synthesis of bioactive molecules, particularly within lipid-based scaffolds and polyketide analogs.
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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: