2,3-Dimethoxybenzyl chloride is an organic compound characterized by its benzyl chloride structure, where two methoxy groups are substituted at the 2 and 3 positions of the benzene ring. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity due to the presence of the benzyl chloride functional group, which can undergo nucleophilic substitution reactions. The methoxy groups enhance the electron density of the aromatic ring, influencing its reactivity and making it a useful intermediate in organic synthesis. It is soluble in organic solvents like dichloromethane and ether but has limited solubility in water. Safety precautions are necessary when handling this compound, as it may be irritating to the skin and eyes, and proper ventilation is recommended due to potential harmful vapors. Its applications include use in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, highlighting its significance in the field of organic chemistry.

2,3-Dimethoxybenzyl chloride

3893-01-4: 1-(Chloromethyl)-2,3-Dimethoxybenzene

2,3-Dimethoxybenzyl chloride is a reactive chlorine compound that can be used to make a variety of organic compounds. The chloride gas is generated through the catalytic reduction of piperidine with hydrogen chloride in the presence of a palladium catalyst. This reaction is mediated by an alkali metal, such as sodium or potassium. The demethylation of 2,3-dimethoxybenzyl chloride can occur by the addition of an alkyl halide and base to give methylene chloride and phenol. The use of 2,3-dimethoxybenzyl chloride has been shown to be effective in treating allergic reactions by inducing hyposensitization.

CAS 3893-01-4: 2,3-Dimethoxybenzyl chloride

2,3-Dimethoxybenzyl chloride

Ref: 3D-DAA89301

2,3-Dimethoxybenzyl Chloride

Ref: 4Z-B-139089

2,3-Dimethoxybenzyl chloride

Ref: 54-OR200026

2,3-Dimethoxybenzyl chloride

Ref: 10-F018573

2,3-DIMETHOXYBENZYL CHLORIDE

Ref: IN-DA00C0OL