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Structure of 89167-34-0
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4-Chloro-3-iodopyridine is a halogenated pyridine derivative featuring complementary reactive sites for cross-coupling transformations. The chlorine and iodine substituents enable sequential functionalization under palladium catalysis, offering precise control in building complex heterocyclic architectures. This compound serves as a key intermediate in medicinal chemistry and materials synthesis, combining high reactivity with bench-stable handling.
4-Chloro-3-iodopyridine serves as a versatile bifunctional building block in cross-coupling chemistry, enabling sequential functionalization at the 3- and 4-positions of the pyridine ring. The chlorine moiety undergoes palladium-catalyzed coupling with boron, tin, or zinc reagents, while the iodide facilitates orthogonal Suzuki, Stille, or Negishi reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science.
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GHS No : GHS05,GHS07,GHS09
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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-H315-H318-H410
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Precautionary Statements : P264-P270-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: