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Structure of 1515925-06-0
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This bench-stable arylamine features a difluoromethoxy group that enhances metabolic stability and modulates electronic properties. The ortho-chlorine substituent introduces steric and electronic influence, enabling precise tuning in medicinal chemistry applications. This scaffold integrates readily into bioactive molecules for drug discovery workflows.
(2-Chloro-6-(difluoromethoxy)phenyl)methanamine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical scaffolds. Its ortho-chloro and difluoromethoxy substituents provide enhanced metabolic stability and modulated lipophilicity. The primary amine functionality facilitates straightforward derivatization via amidation, alkylation, or reductive amination, supporting efficient route development for targeted compound libraries.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: