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Structure of 1214366-31-0
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This bench-stable amine features a fluorinated aromatic ring paired with a methoxy group, enabling enhanced metabolic stability and tunable lipophilicity. The hydrochloride salt form ensures high solubility in aqueous media and simplifies handling in synthetic workflows. Ideal for incorporating into bioactive scaffolds requiring electron-withdrawing substituents and polar functionality.
(2-Fluoro-6-methoxyphenyl)methanamine hydrochloride serves as a versatile building block for medicinal chemistry, enabling the synthesis of bioactive arylamines via standard amine coupling and electrophilic substitution reactions. The ortho-fluoro and para-methoxy substituents provide enhanced metabolic stability and modulate electronic properties, while the hydrochloride salt ensures excellent bench stability and ease of handling. This compound facilitates efficient access to heterocyclic scaffolds and drug-like intermediates through well-established synthetic protocols.
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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-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: