Nom du produit:6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinolin-1(2H)-one

IUPAC Name:6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydroisoquinolin-1-one

CAS:1219130-56-9
Formule moléculaire:C15H18BNO3
Pureté:95%
Numéro de catalogue:CM135945
Poids moléculaire:271.12

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Détails du produit

N° CAS:1219130-56-9
Formule moléculaire:C15H18BNO3
Point de fusion:-
Code SMILES:O=C1NC=CC2=C1C=CC(B3OC(C)(C)C(C)(C)O3)=C2
Densité:
Numéro de catalogue:CM135945
Poids moléculaire:271.12
Point d'ébullition:
N° Mdl:MFCD18426474
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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Isoquinolines
Compared to quinolines, isoquinolines are also prominent structural motifs present in many biologically significant natural and synthetic compounds. Some well-known isoquinoline alkaloids include the anticancer and anticonvulsant berberine, the vasodilator and antispasmodic drugs papaverine and emetine. In addition to naturally occurring isoquinolines, synthetic analogs have also shown significant biological activity.

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