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Structure of 870063-62-0
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(3-Fluoropyridin-4-yl)methanamine features a fluorinated pyridine core paired with a primary amine group, enabling direct functionalization in medicinal chemistry. The electron-deficient heterocycle enhances reactivity in cross-coupling processes, while the pendant amine facilitates conjugation or salt formation. This scaffold integrates readily into bioactive molecules requiring metabolic stability and targeted binding.
(3-Fluoropyridin-4-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling reactions. Its pyridine core provides enhanced metabolic stability and favorable pharmacokinetic properties, while the primary amine facilitates conjugation with electrophiles, including acyl chlorides, aldehydes, and isocyanates. The ortho-fluoro substituent supports directed metalation and enables regioselective functionalization, enhancing synthetic flexibility for scaffold diversification. Bench-stable and readily purified by standard techniques, it functions effectively in both small-molecule synthesis and process development workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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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: