3-Chloro-1,1-dimethoxypropane is an organic compound characterized by its structure, which includes a propane backbone with two methoxy groups and a chlorine atom attached to the third carbon. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic nature. The presence of the chlorine atom makes it a potential candidate for various chemical reactions, including nucleophilic substitutions. Its methoxy groups can also participate in reactions typical of ethers, such as cleavage under acidic conditions. 3-Chloro-1,1-dimethoxypropane is used in organic synthesis and may serve as an intermediate in the production of other chemical compounds. Safety precautions should be observed when handling this substance, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

3-chloro-1,1-dimethoxypropane

35502-06-8: Propane, 3-chloro-1,1-dimethoxy-, 3-Chloro-1,1-dimethoxypropane

3-Chloropropionaldehyde Dimethyl Acetal is a monomer that is used as a stabilizer in hydrocarbons. It has been shown to be an effective catalyst for the stepwise synthesis of hydrocarbons, and can be used to convert methanol into acetone. 3-Chloropropionaldehyde Dimethyl Acetal also reacts with trimethylamine to produce bio-oil, which can be used as a fuel or starting material for other chemical products. 3-Chloropropionaldehyde Dimethyl Acetal is also an acetal that can be synthesized by reacting acetone with trimethylamine. This reaction yields a product with the same molecular weight and stability as propionaldehyde dimethyl acetal, but the addition of chlorine prevents it from becoming too acidic.

CAS 35502-06-8: 3-chloro-1,1-dimethoxypropane

3-Chloropropionaldehyde Dimethyl Acetal

Ref: 3D-KBA50206

3-chloro-1,1-dimethoxy-propane

Ref: IN-DA003J62

3-Chloro-1,1-dimethoxypropane

Ref: 10-F773265

3-Chloropropionaldehyde Dimethyl Acetal

Ref: 3B-C2458