2-Iodo-4,5-dimethoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and two methoxy groups attached to the benzene ring. The presence of the iodine atom at the second position of the ring significantly influences its reactivity and properties. This compound typically appears as a pale yellow to light brown solid and is soluble in organic solvents such as ethanol and dichloromethane, but less soluble in water due to its hydrophobic nature. It is often used in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, owing to its electrophilic properties. The methoxy groups enhance the electron density of the aromatic ring, making it more reactive towards electrophilic substitution reactions. Additionally, the compound may exhibit interesting biological activities, which can be explored in medicinal chemistry. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity and reactivity.

2-Iodo-4,5-dimethoxybenzaldehyde

61203-53-0: 6-Iodoveratraldehyde, Benzaldehyde, 2-Iodo-4,5-Dimethoxy-, 2-Iodo-4,5-dimethoxybenzaldehyde

2-Iodo-4,5-diMethoxybenzaldehyde

2-Iodo-4,5-dimethoxybenzaldehyde (2IDMB) is a reactive intermediate that is used in cross-coupling reactions. It has been shown to efficiently form biaryl compounds with alcohols and phosphonium salts. 2IDMB can be used as a reagent for the synthesis of dibenzofurans, which are medicinally important. The Wittig olefination reaction, which is catalyzed by 2IDMB, allows for the synthesis of triarylbismuths from bismuth carboxylates and alkenes. This process is more efficient than using phosphorus pentachloride as a catalyst.

CAS 61203-53-0: 2-Iodo-4,5-dimethoxybenzaldehyde

2-Iodo-4,5-diMethoxybenzaldehyde

Ref: IN-DA00EKWX

2-Iodo-4,5-dimethoxybenzaldehyde

Ref: 3D-FI16383