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Structure of 51420-25-8
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This bench-stable arylmethanol features a para-amino group flanked by a chloro substituent, enabling direct incorporation into pharmaceutical intermediates and functionalized biaryl scaffolds. The hydroxymethyl functionality supports derivatization under mild conditions, while the electron-donating amino moiety enhances reactivity in coupling processes.
(4-Amino-2-chlorophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling the synthesis of diverse heterocyclic scaffolds and functionalized aryl derivatives. Its dual amino and hydroxymethyl functionalities offer orthogonal reactivity for selective derivatization, while the chloro group facilitates palladium-catalyzed coupling reactions. The compound exhibits good bench stability and is amenable to standard purification techniques, making it well-suited for iterative synthesis workflows in API development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: