CAS 20469-63-0
:1-Iodo-2,4-dimetoxibenzeno
- 1,3-Dimethoxy-4-iodobenzene
- 1-Iodo-2,4-dimethoxybenzene
- 2,4-Dimethoxyiodobenzene
- 2,4-Dimethoxyphenyl iodide
- 2-Iodo-1,5-dimethoxybenzene
- Benzene, 1-iodo-2,4-dimethoxy-
- NSC 89774
2,4-Dimethoxyiodobenzene
CAS:Fórmula:C8H9IO2Pureza:>98.0%(GC)Cor e Forma:White to Almost white powder to crystalPeso molecular:264.061-Iodo-2,4-dimethoxybenzene, 97%
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
Fórmula:C8H9IO2Pureza:97%Cor e Forma:Crystals or powder or crystalline powder or clear liquid as melt, White to cream to yellow to dark brown to pale yellowPeso molecular:264.062,4-Dimethoxy-1-iodobenzene
CAS:2,4-Dimethoxy-1-iodobenzeneFórmula:C8H9IO2Pureza:98%Cor e Forma: faint yellow fused solidPeso molecular:264.06033g/mol2,4-Dimethoxyiodobenzene
CAS:Fórmula:C8H9IO2Pureza:95%Cor e Forma:Solid, Low Melting SolidPeso molecular:264.0622,4-Dimethoxyiodobenzene
CAS:2,4-Dimethoxyiodobenzene is a methyl ketone that has three methoxy groups. It is used as a building block in organic synthesis and can be synthesized by the reaction of 2,4-dimethoxybenzaldehyde with peroxide and methylamine. 2,4-Dimethoxyiodobenzene inhibits radical formation by reacting with an activated metal halide to form a covalent bond between the two molecules. The terminal alkyne reacts with a halogen to form an alkynyl radical which then reacts with another activated metal halide to form a second covalent bond. This process creates a new radical that has been deactivated by the addition of two bonds, preventing it from initiating another chain reaction. 2,4-Dimethoxyiodobenzene also exhibits inhibitory potency against β-amino acid decomposition through the same mechanism.
Fórmula:C8H9IO2Pureza:Min. 95%Peso molecular:264.06 g/mol





