Nom du produit:9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
IUPAC Name:9-octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
- CAS:406726-92-9
- Formule moléculaire:C32H47B2NO4
- Pureté:96%
- Numéro de catalogue:CM136907
- Poids moléculaire:531.34
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:406726-92-9
- Formule moléculaire:C32H47B2NO4
- Point de fusion:-
- Code SMILES:CC1(C)C(C)(C)OB(C2=CC3=C(C=C2)C4=C(C=C(B5OC(C)(C)C(C)(C)O5)C=C4)N3CCCCCCCC)O1
- Densité:
- Numéro de catalogue:CM136907
- Poids moléculaire:531.34
- Point d'ébullition:608.8°C at 760 mmHg
- N° Mdl:MFCD23703114
- 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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