Dimethyl phenylpropanedioate, identified by its CAS number 37434-59-6, is an organic compound characterized by its structure, which includes two ester functional groups derived from phenylpropanedioic acid. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its pleasant aromatic odor, which is characteristic of many esters. Dimethyl phenylpropanedioate is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The compound is often utilized in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the ester groups, making it susceptible to hydrolysis and transesterification reactions. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Proper safety protocols should be followed when working with this substance in a laboratory setting.

dimethyl phenylpropanedioate

37434-59-6: Dimethyl phenylpropanedioate, identified by its CAS number 37434-59-6, is an organic compound characterized by its structure, which includes two ester functional groups derived from phenylpropanedioic acid. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its pleasant aromatic odor, which is characteristic of many esters. Dimethyl phenylpropanedioate is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The compound is often utilized in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the ester groups, making it susceptible to hydrolysis and transesterification reactions. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Proper safety protocols should be followed when working with this substance in a laboratory setting.

Dimethyl 2-phenylmalonate

<p>1,3-Dimethyl 2-phenylpropanedioate is a molecule that is used in the production of malonic acid. The reaction mechanism involves an enzymatic homogenization of the reactants, which leads to the formation of carbonyl oxygens and reaction intermediates. The carbonyl oxygens are then protonated by ethyl diazoacetate to form allyl carbonates. This process occurs in the presence of immobilized enzymes and chemical reactions.</p>

CAS 37434-59-6

dimethyl phenylpropanedioate

Dimethyl 2-phenylmalonate

Ref: 54-OR55027

1,3-Dimethyl 2-phenylpropanedioate

Ref: 3D-MBA43459