CAS 19099-54-8
:1-Iod-2-isopropylbenzol
- 1-Iodo-2-(1-methylethyl)benzene
- 1-Iodo-2-(Propan-2-Yl)Benzene
- 1-Iodo-2-isopropylbenzene
- 1-Iodo-2-propan-2-ylbenzene
- 2-Iodo-1-isopropylbenzene
- 2-Iodocumene~2-Isopropyliodobenzene
- 2-Isopropyl-1-iodobenzene
- 2-Isopropyliodobenzene
- 2-Isopropylphenyl iodide
- Benzene, 1-iodo-2-(1-methylethyl)-
- Cumene, o-iodo-
- o-Iodocumene
- 2-IODOCUMENE
- 2-IODOISOPROPYLBENZENE
- 1-IODO-2-ISOPROPYL BENZENE 95%
- Iodocumene
- Weitere Synonyme anzeigen
2-Iodocumene
CAS:Formel:C9H11IReinheit:>98.0%(GC)Farbe und Form:Light yellow to Brown clear liquidMolekulargewicht:246.091-Iodo-2-isopropylbenzene, 95%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formel:C9H11IReinheit:95%Farbe und Form:Liquid, Clear, colorless to yellow or orange/brown or red/brownMolekulargewicht:246.09Benzene, 1-iodo-2-(1-methylethyl)-
CAS:Formel:C9H11IReinheit:97%Farbe und Form:LiquidMolekulargewicht:246.08812-Isopropyliodobenzene
CAS:2-IsopropyliodobenzeneReinheit:97%Farbe und Form:LiquidMolekulargewicht:246.09g/mol2-Iodocumene
CAS:Kontrolliertes ProduktFormel:C14H16N2·HClFarbe und Form:NeatMolekulargewicht:248.7512-Iodocumene
CAS:2-Iodocumene is a chemical that belongs to the group of unsymmetrical carbonyl compounds. It is an intermediate in the synthesis of saccharin and other organic chemicals, as well as in the production of pharmaceuticals. 2-Iodocumene can be used as a ligand in metal-catalyzed cross-coupling reactions between organometallic reagents and various types of electrophiles. This compound has been shown to react with iron at room temperature to form an active catalyst for the regioselective cleavage of C-C bonds. The mechanistic studies have revealed that 2-iodocumene acts as an electron acceptor and a nucleophile, which allows it to act as a bifunctional catalyst during these reactions. The reaction rate depends on steric hindrance, which may be due to the presence of carbonyl groups or cyclic structures. The mechanism is supported by computational studies using density functional
Formel:C9H11IReinheit:Min. 95%Molekulargewicht:246.09 g/mol






