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Structure of 2173991-78-9
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This bicyclic scaffold delivers a rigid, sterically constrained aminomethyl handle ideal for peptide conjugation and macrocyclization. The hydrochloride salt enhances solubility and stability under standard bench conditions, enabling seamless integration into synthetic workflows requiring precise spatial control and enhanced metabolic resilience.
3-(Aminomethyl)bicyclo[1.1.1]pentane-1-carboxylic acid hydrochloride serves as a rigid, conformationally constrained bioisostere of the alanine side chain, enabling precise spatial positioning in peptide-based drug discovery. The bicyclic core imparts high metabolic stability and enhanced membrane permeability, while the pendant primary amine and carboxylic acid facilitate standard coupling reactions and salt formation. Its bench-stable form simplifies handling in solid-phase synthesis and medicinal chemistry workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: