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Structure of 1256790-45-0
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6-Bromo-2-methoxynicotinonitrile features a bromine atom at the 6-position and a methoxy group at the 2-position on a nicotinonitrile scaffold, delivering a sterically accessible site for cross-coupling. The electron-deficient pyridine core enhances reactivity in transition-metal-catalyzed transformations. This bench-stable building block enables efficient access to functionalized heterocycles in medicinal chemistry and materials synthesis.
6-Bromo-2-methoxynicotinonitrile serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. Its bromo group facilitates Suzuki-Miyaura and Stille couplings, while the nitrile and methoxy functionalities offer orthogonal handles for further functionalization. The compound exhibits excellent bench stability and is compatible with standard reaction conditions, simplifying purification and scalability in API development workflows.
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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: