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Structure of 3721-95-7
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Cyclobutanecarboxylic acid features a strained four-membered ring that imparts unique reactivity and conformational rigidity. This structural motif enhances its utility in synthetic routes requiring defined stereochemistry or ring fusion. The carboxylic acid group enables direct functionalization or derivatization under standard conditions, making it valuable for building complex molecular architectures in medicinal chemistry and materials science.
Cyclobutanecarboxylic acid serves as a valuable building block in medicinal chemistry and synthetic organic chemistry, offering a rigid, strained cyclobutane scaffold that enhances metabolic stability and bioavailability in drug candidates. Its carboxylic acid functionality enables direct derivatization into amides, esters, and acyl chlorides, facilitating downstream conjugation and incorporation into complex molecular architectures. The compound exhibits good bench stability and is compatible with standard functional group manipulations, making it well-suited for iterative synthesis workflows and API development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H227-H314
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Precautionary Statements : P210-P260-P264-P280-P301+P330+P331-P304+P340-P363-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: