(3-methoxypyridin-4-yl)boronic acid hydrate


Chemical Name: (3-methoxypyridin-4-yl)boronic acid hydrate
CAS Number: 1072952-50-1
Product Number: AG003BSQ(AGN-PC-0WAIWC)
Synonyms:
MDL No:
Molecular Formula: C6H10BNO4
Molecular Weight: 170.9589

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P340-P332+P313-P337+P313-P340-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-Methoxypyridin-4-yl)boronic acid hydrate is a versatile compound used extensively in chemical synthesis, particularly in the field of organic chemistry. With its unique properties and reactivity, this boronic acid derivative serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.In organic synthesis, (3-Methoxypyridin-4-yl)boronic acid hydrate is commonly employed in Suzuki-Miyaura cross-coupling reactions. This powerful method allows for the formation of carbon-carbon bonds, enabling the rapid assembly of complex molecular structures. By incorporating this boronic acid into the reaction, chemists can selectively introduce the 3-methoxypyridin-4-yl functional group into target molecules with high efficiency.Furthermore, the presence of the boron atom in (3-Methoxypyridin-4-yl)boronic acid hydrate offers additional versatility in chemical transformations. The boronic acid moiety can participate in various reactions such as hydrolysis, oxidation, and reduction, expanding the synthetic possibilities for researchers. This compound's compatibility with a wide range of functional groups and reaction conditions makes it an invaluable tool for the preparation of novel molecules with diverse structures and properties.Overall, (3-Methoxypyridin-4-yl)boronic acid hydrate plays a crucial role in modern chemical synthesis, facilitating the efficient construction of complex organic molecules for various applications in the fields of medicine, agriculture, and materials science.