Dimethylstilbene refers to a group of organic compounds derived from stilbene, characterized by the presence of two methyl groups attached to the stilbene structure. The compound with the CAS number 18869-29-9 specifically denotes 4,4'-dimethylstilbene, which features two methyl groups at the para positions of the phenyl rings. This compound is a colorless to pale yellow solid at room temperature and is known for its stability and resistance to heat. Dimethylstilbene exhibits properties typical of aromatic compounds, including a relatively high melting point and low solubility in water, but good solubility in organic solvents. It is primarily used in research and industrial applications, particularly in the synthesis of polymers and as a precursor in organic synthesis. Additionally, dimethylstilbene has been studied for its potential biological activity, including its effects on estrogen receptors, which has implications in the field of endocrinology and toxicology. However, safety and handling precautions are necessary due to its potential health effects.

Dimethylstilbene

18869-29-9: 4,4-Dimethyl-trans-stilbene, 1,1'-(E)-ethene-1,2-diylbis(4-methylbenzene), (E)-1,2-Bis(4-methylphenyl) ethene

Benzene, 1,1'-(1E)-1,2-ethenediylbis[4-methyl-

4,4'-Dimethyl-trans-stilbene is a compound that belongs to the class of fatty acids. It is a product of the oxidation of ethyl diazoacetate with an irradiation process. The mechanism of this reaction is via a liquid phase oxidation catalyst and methyl ethyl trans-stilbene. 4,4'-Dimethyl-trans-stilbene has been shown to produce phenyl groups and vibrational progressions when subjected to fluorescence spectroscopy. This product also has functional groups such as terephthalic acid and polycarboxylic acid sulfoxide.

CAS 18869-29-9: Dimethylstilbene

Benzene, 1,1'-(1E)-1,2-ethenediylbis[4-methyl-

Ref: IN-DA002H62

4,4'-Dimethyl-trans-stilbene

Ref: 3D-TAA86929

4,4'-Dimethyl-trans-stilbene

Ref: 3B-D2708

(E)-1,2-Di-p-tolylethene

Ref: 10-F544858