製品名:[1,5]naphthyridine-3-boronic acid

IUPAC Name:(1,5-naphthyridin-3-yl)boronic acid

CAS番号:1443112-44-4
分子式:C8H7BN2O2
純度:95%
カタログ番号:CM105205
分子量:173.97

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CM105205-1g 1-2 Weeks ȋǠȋȤ

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製品詳細

CAS番号:1443112-44-4
分子式:C8H7BN2O2
融点:-
SMILESコード:OB(O)C1=CC2=NC=CC=C2N=C1
密度:
カタログ番号:CM105205
分子量:173.97
沸点:
MDL番号:
保管方法:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Naphthyridines
Naphthyridine is a class of aromatic heterocyclic compounds whose chemical formula is C8H6N2. They consist of naphthalene bicyclic rings in which two carbon atoms are replaced by nitrogen atoms. There are ten isomers of naphthyridine, because naphthyridine has two benzene rings, has strong π-π conjugation, and has better luminescence properties. Common naphthyridines are 1,8-naphthyridines. There are many kinds of 1,8-naphthyridine derivatives, and they are widely used.