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Structure of 115514-77-7
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3-Chloro-4-methoxy-benzylamine features a benzylamine scaffold substituted with electron-donating methoxy and electron-withdrawing chloro groups at the meta and para positions, respectively. This electronic asymmetry enhances its reactivity in nucleophilic coupling processes. The compound exhibits bench-stable handling characteristics and integrates readily into synthetic routes for bioactive molecule construction.
3-Chloro-4-methoxy-benzylamine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and functionalized arylamines. Its ortho-chloro and para-methoxy substituents provide orthogonal reactivity for downstream coupling and derivatization. The amine functionality facilitates easy purification and conjugation, while the benzyl scaffold offers enhanced metabolic stability. This compound functions reliably in standard amide coupling, Suzuki-Miyaura, and electrophilic substitution protocols.
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GHS Pictogram :
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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 : Ⅲ
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Hazard Statements : H314-H318
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Precautionary Statements : P280-P302+P352
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Lot numbers can be found on the outside label of a product: