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Structure of 1020173-27-6
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4-Amino-3-fluoro-2-methylphenol features a strategically positioned amino group adjacent to a fluorine substituent, enabling enhanced electron donation and directed reactivity. The ortho-methyl group provides steric stabilization, while the phenolic hydroxyl offers a handle for derivatization. This scaffold combines electronic tuning with bench-stable handling, making it valuable in medicinal chemistry and agrochemical synthesis.
4-Amino-3-fluoro-2-methylphenol serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated heterocycles and bioactive scaffolds. Its ortho-directed reactivity facilitates efficient functionalization, while the amino and phenolic groups offer complementary handles for derivatization. Bench-stable and readily purified, it functions effectively in standard coupling and cyclization 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: