Nom du produit:[1,5]naphthyridine-3-boronic acid

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

CAS:1443112-44-4
Formule moléculaire:C8H7BN2O2
Pureté:95%
Numéro de catalogue:CM105205
Poids moléculaire:173.97

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CM105205-1g 1-2 Weeks ŴǧŴƻ

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Détails du produit

N° CAS:1443112-44-4
Formule moléculaire:C8H7BN2O2
Point de fusion:-
Code SMILES:OB(O)C1=CC2=NC=CC=C2N=C1
Densité:
Numéro de catalogue:CM105205
Poids moléculaire:173.97
Point d'ébullition:
N° Mdl:
Stockage:

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.