Nom du produit:(9H-Carbazol-1-yl)boronic acid
IUPAC Name:(9H-carbazol-1-yl)boronic acid
- CAS：869642-36-4
- Formule moléculaire：C12H10BNO2
- Pureté：95%
- Numéro de catalogue：CM217681
- Poids moléculaire：211.03
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:869642-36-4
- Formule moléculaire:C12H10BNO2
- Point de fusion:-
- Code SMILES:OB(C1=CC=CC2=C1NC3=C2C=CC=C3)O
- Densité:
- Numéro de catalogue:CM217681
- Poids moléculaire:211.03
- 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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- Carbazoles
- Carbazoles are an important class of nitrogen-containing heterocycles with a planar tricyclic skeleton consisting of two benzene rings fused on both sides of the central pyrrole ring, with a large aromatic system and a central nitrogen atom, showing broad of electron delocalization. The structure of this compound is based on the indole structure, but in which a second benzene ring is fused to a five-membered ring at positions 2-3 of the indole. Carbazole structural motifs are widely found in, but not limited to, a large number of natural alkaloids of plant or bacterial origin. Since many of these alkaloids are medically useful, exhibit a fairly wide range of biological activities (anticancer, anti-HIV, antibacterial, anti-Alzheimer's disease, anticoagulant, analgesic, antiepileptic, antidiabetic, antioxidant, etc.). Medicinal chemistry also uses carbazole motifs in synthetic drugs to combat hypertension, heart disease, and hepatitis C virus replication.
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