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Structure of 675126-27-9
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This boronate moiety integrates a methoxy-substituted aromatic core with a morpholinopropoxy side chain, delivering enhanced solubility and metabolic stability. The para-nitro group enables efficient coupling in Suzuki-Miyaura reactions, while the amino functionality offers direct derivatization potential for probe development.
2-Amino-4-methoxy-5-(3-morpholinopropoxy)benzonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted benzimidazoles and quinoline scaffolds. The ortho-amino and nitrile groups facilitate cyclization under mild conditions, while the methoxy and morpholinopropoxy substituents provide solubility and modulate electronic properties. Bench-stable and compatible with standard purification protocols, it functions effectively in multi-step medicinal chemistry campaigns requiring functional group tolerance and predictable reactivity.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: