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Structure of 134234-04-1
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This cyclopentene derivative features a strategically positioned amino group and carboxylic acid moiety, enabling direct incorporation into bioactive scaffolds. The rigid, unsaturated backbone provides conformational constraint, while the amine facilitates derivatization under standard conditions. Ideal for probing structure-activity relationships in medicinal chemistry.
(1S,4R)-4-Aminocyclopent-2-enecarboxylic acid serves as a valuable chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. Its conjugated enamine-carboxylic acid architecture enables facile functionalization via Michael addition, electrophilic substitution, and coupling reactions. The stereochemistry at C1 and C4 ensures high diastereoselectivity in downstream transformations, while the molecule exhibits good bench stability and ease of purification, making it well-suited for medicinal chemistry campaigns and process-scale applications.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: