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Structure of 931105-37-2
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Methyl 5-bromo-2-fluoronicotinate is a fluorinated heterocyclic ester featuring complementary halogen substituents at the 5- and 2-positions of the nicotinate core. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions, offering high regioselectivity and stability under standard conditions. The molecule integrates readily into synthetic sequences requiring precise substitution patterns.
Methyl 5-bromo-2-fluoronicotinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromine at C5 facilitates Suzuki, Stille, or Negishi couplings, while the fluorine at C2 enhances electrophilicity for nucleophilic substitution. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis of substituted nicotinates and pharmaceutical intermediates.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: