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Structure of 38275-57-9
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5-Bromopyrimidine-2-carbonitrile serves as a key heterocyclic building block for medicinal chemistry and materials science. The molecule combines a bromine substituent at the 5-position with a nitrile group at C2, enabling selective cross-coupling reactions and facilitating downstream functionalization. This dual-reactive motif supports efficient access to complex pyrimidine derivatives under standard conditions.
5-Bromopyrimidine-2-carbonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine and nitrile functionalities. The electron-deficient pyrimidine core facilitates nucleophilic substitution and supports the construction of heterocyclic scaffolds. Its bench-stable nature and compatibility with diverse functional groups make it ideal for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS05,GHS09,GHS07
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H315-H318-H332-H335-H410
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Precautionary Statements : P260-P261-P264-P270-P271-P273-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P363-P391-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: