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Structure of 205877-13-0
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This bench-stable phenolic alcohol features a strategically positioned amino group and methoxy substituent, enabling direct integration into bioactive scaffolds. The hydroxymethyl moiety offers a versatile handle for derivatization, while the electron-donating methoxy group enhances solubility and reactivity in synthetic transformations.
(2-Amino-3-methoxyphenyl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocycles and pharmaceutical intermediates. Its ortho-amino and methoxy functionalities provide orthogonal reactivity for selective derivatization, while the benzylic alcohol supports straightforward functionalization via oxidation or protection. The compound exhibits excellent bench stability and compatibility with standard synthetic protocols, facilitating purification and integration into multi-step sequences.
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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: