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Structure of 39201-33-7
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4-Cyanobutanoic acid integrates a nitrile group at the γ-position relative to the carboxylic acid, enabling direct functionalization in synthetic routes. This electron-withdrawing moiety enhances reactivity for nucleophilic additions and facilitates derivatization under standard conditions. The molecule exhibits robust stability and convenient handling, making it valuable for building complex heterocycles and bioactive scaffolds in medicinal chemistry and materials science applications.
4-Cyanobutanoic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to γ-aminobutyric acid (GABA) derivatives and heterocyclic scaffolds via cyclization or hydrolysis. Its bifunctional nature—combining a nitrile and carboxylic acid group—facilitates orthogonal transformations, while its bench stability supports reliable handling in multi-step syntheses. Functions effectively in coupling reactions and serves as a key intermediate in the development of bioactive molecules and pharmaceutical candidates.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2923
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Class : 8,6.1
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Packing Group : Ⅲ
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Hazard Statements : H319
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Precautionary Statements : P264-P280-P305+P351+P338
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Lot numbers can be found on the outside label of a product: