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Structure of 98645-43-3
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2-Chloro-4-methoxynicotinonitrile features a strategically positioned nitrile group and chloro substituent on a pyridine scaffold, enabling direct integration into heterocyclic scaffolds. The methoxy functionality enhances solubility and modulates electronic properties, supporting efficient coupling in synthetic sequences under standard conditions.
2-Chloro-4-methoxynicotinonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds via nucleophilic displacement and cross-coupling reactions. The ortho-chloro group facilitates regioselective functionalization, while the nitrile and methoxy substituents offer complementary reactivity for downstream transformations. Its bench stability and compatibility with standard reaction conditions make it ideal for modular synthesis of bioactive heterocycles and API intermediates.
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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: