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Structure of 430-99-9
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2-Fluoroacrylic acid serves as a versatile building block for fluorinated α,β-unsaturated systems, enabling efficient Michael additions and Diels–Alder reactions. Its conjugated enoic acid functionality exhibits enhanced electrophilicity at the β-position, facilitating selective nucleophilic attack under mild conditions. The molecule demonstrates bench stability and compatibility with common protecting groups, supporting straightforward purification and integration into synthetic sequences targeting bioactive heterocycles and pharmaceutical intermediates.
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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#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: