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Structure of 74896-24-5
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4-Amino-3,5-dimethylbenzonitrile features a para-amino group flanked by two methyl substituents on a nitrile-bearing aromatic ring. This electron-rich scaffold integrates readily into heterocyclic systems and serves as a key intermediate in pharmaceutical synthesis. The nitrile moiety enables further functionalization via nucleophilic addition or reduction.
4-Amino-3,5-dimethylbenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles and other heterocyclic scaffolds. The ortho-dimethyl substitution enhances steric control during coupling reactions, while the nitrile group offers direct functionalization potential via hydrolysis or nucleophilic addition. Bench-stable and readily purified by recrystallization, it functions effectively in standard amide formation, Suzuki-Miyaura, and Ullmann-type transformations.
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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: