Nom du produit:6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazoline

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

CAS:1375301-92-0
Formule moléculaire:C14H17BN2O2
Pureté:95%
Numéro de catalogue:CM135101
Poids moléculaire:256.11

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Détails du produit

N° CAS:1375301-92-0
Formule moléculaire:C14H17BN2O2
Point de fusion:-
Code SMILES:CC1(C)C(C)(C)OB(C2=CC3=CN=CN=C3C=C2)O1
Densité:
Numéro de catalogue:CM135101
Poids moléculaire:256.11
Point d'ébullition:
N° Mdl:MFCD11521590
Stockage:

Category Infos

Quinazolines
Quinazolines belong to heterocyclic chemistry, also known as 1,3-naphthalenes. The backbone consists of two six-membered aromatic rings fused to each other, with two nitrogen atoms at positions 1 and 3 on the backbone. The presence of these two nitrogen atoms in quinazoline increases its importance in pharmaceutical and biological reactions. Quinazolines and their derivatives are among the most important heterocyclic compounds due to their diverse chemical reactivity and important range of biological activities.
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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