
Catalog Number	AR01AAF7
Chemical Name	5-Isothiocyanato-2-methoxypyridine
CAS Number	52023-93-5
Molecular Formula	C7H6N2OS
Molecular Weight	166.2003
MDL Number	MFCD11131118
SMILES	S=C=Nc1ccc(nc1)OC

5-Isothiocyanato-2-methoxypyridine is a versatile chemical compound widely utilized in chemical synthesis for its unique reactivity and functional properties. As an isothiocyanate derivative, it is particularly valued for its ability to act as a sulfur donor in various reactions, making it a valuable reagent in organic synthesis. Its methoxy group provides additional versatility, allowing for selective modifications and functionalizations in target molecules.In chemical synthesis, 5-Isothiocyanato-2-methoxypyridine serves as a key building block in the preparation of various heterocyclic compounds, such as pyridine and pyrimidine derivatives. Its isothiocyanate moiety can undergo nucleophilic substitution reactions with a variety of nucleophiles, enabling the introduction of sulfur-containing groups into organic molecules. This reactivity makes it a useful tool in the synthesis of pharmaceuticals, agrochemicals, and materials chemistry.Furthermore, the unique combination of the isothiocyanate and methoxy groups in 5-Isothiocyanato-2-methoxypyridine allows for the formation of complex structures with diverse functionalities. By carefully selecting reaction conditions and partners, chemists can access a wide range of functionalized products, making this compound a valuable asset in the toolbox of synthetic chemists.

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GHS Pictogram
Signal Word	Danger
UN#	2811
Hazard Statements	H315-H317-H319-H330-H334-H335-H351-H412
Precautionary Statements	P201-P202-P260-P264-P271-P272-P273-P280-P284-P302+P352-P304+P340+P310-P305+P351+P338-P308+P313-P333+P313-P337+P313-P403+P233-P405-P501
Class	6.1
Packing Group	Ⅲ