Some scientific research about Naphthalen-1-ylboronic acid

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Application of 13922-41-3, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 13922-41-3, Name is Naphthalen-1-ylboronic acid, SMILES is C1=CC=C2C(=C1)C(=CC=C2)B(O)O, belongs to naphthyridine compound. In a article, author is Bodrin, Georgy V., introduce new discover of the category.

The first application of the Friedlander reaction for the synthesis of [1,8]naphthyridine derivatives containing phosphorus

The first 2,3-alkylenesubstituted [1,8]naphthyridines bearing a phosphorus moiety have been synthesised by the Friedlander annulations of 2-aminonicotinaldehyde 1 with 2-diphenylphosphoryl(thiophosphoryl)cyclopentanones 7-9.

Application of 13922-41-3, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 13922-41-3.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem