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Structure of 1803595-15-4
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This difluoromethylcyclopropane derivative features a sterically constrained cyclopropane ring bearing a difluoromethyl group and a primary amine, stabilized as its hydrochloride salt. The electron-withdrawing fluorine atoms enhance metabolic stability while preserving nucleophilic reactivity of the amine. This bench-stable crystalline solid integrates readily into medicinal chemistry libraries for probing bioisosteric effects in CNS-targeted compounds.
1-(Difluoromethyl)cyclopropan-1-amine hydrochloride serves as a versatile building block for fluorinated bioactive molecules, enabling direct incorporation of the difluoromethyl group into medicinal chemistry scaffolds. The cyclopropane ring imparts conformational rigidity, while the amine functionality facilitates straightforward derivatization and salt formation. Its bench-stable hydrochloride form ensures ease of handling, purification, and compatibility with standard peptide coupling and reductive amination protocols in synthetic 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: