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Structure of 146038-53-1
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This strained bicyclic scaffold features a fluorinated cage that imparts enhanced metabolic stability and lipophilicity. The carboxylic acid functionality enables direct conjugation or salt formation, facilitating integration into bioactive molecules. Designed for probe development and medicinal chemistry, it offers a rigid, three-dimensional core with improved membrane permeability.
3-Fluorobicyclo[1.1.1]pentane-1-carboxylic acid serves as a rigid, electron-withdrawing building block for medicinal chemistry and agrochemical discovery. Its strained bicyclic scaffold imparts high metabolic stability and conformational restriction, enabling precise spatial positioning of functional groups. The carboxylic acid moiety facilitates direct derivatization or salt formation, while the fluorine substituent enhances lipophilicity and modulates electronic properties. This compound demonstrates excellent bench stability and compatibility with standard coupling reactions, making it a practical tool for constructing bioactive molecules through robust, scalable synthetic routes.
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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 : H315-H318-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P312-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: