Pyridine, 2,3-dichloro-5-iodo-


Chemical Name: Pyridine, 2,3-dichloro-5-iodo-
CAS Number: 97966-01-3
Product Number: AG00H6X3(AGN-PC-03HB21)
Synonyms:
MDL No:
Molecular Formula: C5H2Cl2IN
Molecular Weight: 273.8865

Identification/Properties


Properties
BP:
6.812 °C at 760 mmHg
Storage:
2-8℃;Light sensitive;Inert atmosphere;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,3-Dichloro-5-iodopyridine is a versatile chemical compound that finds extensive application in chemical synthesis processes. Due to its unique structure and reactivity, this compound is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.In organic synthesis, 2,3-Dichloro-5-iodopyridine serves as a valuable substrate for cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to introduce specific functional groups onto the pyridine ring. This compound's halogen atoms can undergo substitution reactions, enabling the modification of its structure to tailor the desired properties of the final product.Additionally, 2,3-Dichloro-5-iodopyridine is utilized in the preparation of heterocyclic compounds, which are essential building blocks in medicinal chemistry. By incorporating this compound into the synthetic route, chemists can access a diverse range of bioactive molecules with potential pharmaceutical applications.Overall, the strategic incorporation of 2,3-Dichloro-5-iodopyridine in chemical synthesis enables the efficient construction of complex molecules, making it a valuable tool for researchers and synthetic chemists in drug discovery and material science.