2,5-Dimethoxybenzoyl chloride is an organic compound characterized by its benzoyl chloride functional group attached to a benzene ring that has two methoxy groups at the 2 and 5 positions. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity due to the presence of the acyl chloride functional group, which makes it a useful intermediate in organic synthesis. It is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water. The presence of methoxy groups enhances its electron-donating properties, influencing its reactivity and stability. 2,5-Dimethoxybenzoyl chloride is often utilized in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals, where it can participate in acylation reactions. However, it should be handled with care due to its corrosive nature and potential to release hydrochloric acid upon hydrolysis. Proper safety precautions, including the use of personal protective equipment, are essential when working with this compound.

2,5-Dimethoxybenzoyl chloride

17918-14-8: 2,5-Dimethoxybenzoyl chloride, 2,5-Dimethoxyphenylcarbonyl chloride, Benzoyl chloride, 2,5-dimethoxy-

2,5-Dimethoxy-benzoyl chloride is a phenolic compound that is synthesized in the laboratory. It has been shown to be a potent neoflavanoid that can be used to treat bacterial and fungal infections. 2,5-Dimethoxy-benzoyl chloride is also effective at inhibiting the growth of cancer cells and has shown anti-inflammatory properties. The molecule was first identified in a natural product from the bark of an African tree (Xanthoceras sorbifolia) in 2006. This compound has been shown to have a conformational change when bound to DNA, which may lead to its anticancer activity.

CAS 17918-14-8: 2,5-Dimethoxybenzoyl chloride

2,5-Dimethoxybenzoyl chloride

Ref: 54-OR26069

2,5-Dimethoxy-benzoyl chloride

Ref: 3D-SAA91814

2,5-Dimethoxy-benzoyl chloride

Ref: 10-F014693

Benzoyl chloride, 2,5-dimethoxy-

Ref: IN-DA0026UG