Phenol, 3-chloro-4-methoxy- is an organic compound characterized by the presence of a phenolic hydroxyl group, a chlorine atom, and a methoxy group attached to a benzene ring. The chlorine atom is located at the meta position relative to the hydroxyl group, while the methoxy group is positioned at the para location. This compound typically exhibits properties common to phenolic compounds, such as moderate solubility in water and higher solubility in organic solvents due to the presence of the methoxy group, which enhances its lipophilicity. It may display weak acidic behavior due to the hydroxyl group, allowing it to participate in hydrogen bonding. The presence of the chlorine substituent can influence its reactivity, making it a potential candidate for various chemical reactions, including electrophilic aromatic substitution. Additionally, the compound may have applications in the synthesis of pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Safety precautions should be observed when handling this compound, as it may pose health risks.

Phenol, 3-chloro-4-methoxy-

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3-Chloro-4-methoxyphenol is an organic compound that is used as a precursor to other chemicals. It can be produced by chlorinating 4-methoxybenzaldehyde, which is a carbon source. The reaction requires activation energy and can be done in the presence of a base. 3-Chloro-4-methoxyphenol has been used to synthesize enantiopure compounds with high mass spectrometric purity. It is reactive and can react with nucleophiles such as water or alcohols, forming hydrolysis process products.

CAS 18093-12-4: Phenol, 3-chloro-4-methoxy-

3-Chloro-4-methoxyphenol

Ref: 3D-TAA09312

3-Chloro-4-methoxyphenol

Ref: 54-OR900665

3-Chloro-4-methoxyphenol

Ref: 10-F545939

Phenol, 3-chloro-4-methoxy-

Ref: IN-DA0022HS