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565237-06-1

(4-iodopyridin-2-yl)methanol

Catalog#: AR01DL8M  |   CAS#: 565237-06-1  |   MDL#: MFCD27925583  |   MF: C6H6INO  |   MW: 235.0224

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Catalog Number AR01DL8M
Chemical Name (4-iodopyridin-2-yl)methanol
CAS Number 565237-06-1
Molecular Formula C6H6INO
Molecular Weight 235.0224
MDL Number MFCD27925583
SMILES OCc1cc(I)ccn1

(4-Iodopyridin-2-yl)methanol is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. With its distinctive structure containing both a pyridine ring and an alcohol group, this compound serves as a valuable building block in the creation of various organic molecules.One of the prominent applications of (4-Iodopyridin-2-yl)methanol is in the synthesis of pharmaceuticals and agrochemicals. Its iodine-substituted pyridine ring provides a valuable site for further functionalization, allowing for the introduction of various functional groups to tailor the properties of the final product. Additionally, the alcohol group can undergo various chemical transformations, enabling the formation of complex molecular structures essential for drug discovery and development.Furthermore, the presence of the iodine atom in (4-Iodopyridin-2-yl)methanol enhances its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling and Heck reaction, facilitating the construction of carbon-carbon and carbon-heteroatom bonds. This reactivity expands the synthetic utility of this compound, making it a valuable tool in the construction of diverse chemical entities.Overall, (4-Iodopyridin-2-yl)methanol plays a crucial role in chemical synthesis by serving as a key intermediate in the preparation of biologically active compounds, functional materials, and other complex organic molecules. Its versatility, reactivity, and compatibility with various synthetic methodologies make it an essential component in the toolkit of organic chemists.
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