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Structure of 1020087-88-0
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This cyclopropylamine derivative features a pyridin-3-yl group directly attached to the cyclopropyl ring, delivering enhanced electron delocalization and improved solubility in polar solvents. The primary amine functionality enables straightforward derivatization for medicinal chemistry applications. Bench-stable under standard conditions, it serves as a key scaffold in bioactive molecule synthesis.
(1-(Pyridin-3-yl)cyclopropyl)methanamine serves as a versatile building block for bioactive molecule synthesis, offering a rigid cyclopropyl scaffold with orthogonal nitrogen functionality. Its pyridyl group enables metal-catalyzed coupling reactions and coordination in transition metal complexes, while the primary amine facilitates derivatization via acylation, alkylation, or reductive amination. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: