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Structure of 1003711-35-0
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2-Bromo-5-cyano-4-picoline features a bromine substituent at the 2-position and a cyano group at the 5-position on a picoline scaffold, delivering high reactivity in cross-coupling transformations. The electron-deficient aromatic core enhances compatibility with palladium catalysis, enabling efficient C–C bond formation under mild conditions. This bench-stable compound serves as a key intermediate in medicinal chemistry and materials synthesis.
2-Bromo-5-cyano-4-picoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its compatible bromo and cyano functionalities. The electron-deficient pyridine core enhances reactivity in nucleophilic substitution processes, while the cyano group offers stability and potential for downstream transformations. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for constructing complex heterocyclic scaffolds in API development.
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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: