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Structure of 6480-66-6
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2,6-Dichloro-4-methoxyaniline features a chlorinated aromatic core with a methoxy group at the para position, delivering enhanced electron donation and steric shielding. This configuration improves stability under reaction conditions and facilitates selective coupling in pharmaceutical intermediates. The molecule integrates readily into heterocyclic systems via nucleophilic substitution, enabling efficient access to complex scaffolds.
2,6-Dichloro-4-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling the construction of heterocyclic scaffolds via standard coupling reactions. Its ortho-chloro groups facilitate selective functionalization, while the methoxy substituent provides electronic modulation and enhanced solubility. The compound exhibits good bench stability and is compatible with common reaction conditions, facilitating efficient purification and integration into multi-step synthetic 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: