CAS 728-87-0
:4-Methoxy-α-(4-methoxyphenyl)benzenemethanol
Description:
4-Methoxy-α-(4-methoxyphenyl)benzenemethanol, also known by its CAS number 728-87-0, is an organic compound characterized by its complex aromatic structure. It features two methoxy groups (-OCH3) attached to a phenyl ring, which enhances its solubility in organic solvents and contributes to its chemical reactivity. The presence of the hydroxyl group (-OH) in the benzenemethanol portion indicates that it can participate in hydrogen bonding, influencing its physical properties such as boiling and melting points. This compound is typically a white to off-white solid at room temperature and is soluble in organic solvents like ethanol and acetone. Its molecular structure suggests potential applications in pharmaceuticals, particularly as a precursor or intermediate in the synthesis of more complex molecules. Additionally, the methoxy groups may impart certain biological activities, making it of interest in medicinal chemistry. However, detailed studies on its specific biological properties and applications would be necessary to fully understand its potential uses.
Formula:C15H16O3
InChI:InChI=1S/C15H16O3/c1-17-13-7-3-11(4-8-13)15(16)12-5-9-14(18-2)10-6-12/h3-10,15-16H,1-2H3
InChI key:InChIKey=ZODAOVNETBTTJX-UHFFFAOYSA-N
SMILES:C(O)(C1=CC=C(OC)C=C1)C2=CC=C(OC)C=C2
Synonyms:- 4,4-Dimethoxydiphenylmethanol
- 4,4′-Dimethoxydiphenylcarbinol
- 4-Methoxy-4′-methoxybenzhydrol
- 4-Methoxy-Α-(4-Methoxyphenyl)Benzenemethanol
- Benzenemethanol, 4-methoxy-α-(4-methoxyphenyl)-
- Benzhydrol, 4,4′-dimethoxy-
- Bis(4-Methoxyphenyl)Methanol
- Bis(4-methoxyphenyl) carbinol
- Bis(p-methoxyphenyl)carbinol
- Bis(p-methoxyphenyl)methanol
- NSC 5256
- p,p′-Dimethoxybenzhydrol
- See more synonyms
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Found 8 products.
4,4'-Dimethoxybenzhydrol
CAS:Formula:C15H16O3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:244.294,4'-Dimethoxybenzhydrol, 98+%
CAS:<p>4,4?-Dimethoxybenzhydrol was used to study the kinetics and mechanism of oxidation of substituted benzhydrols to corresponding benzophenones in the presence of Hg(OAc)2 by N-bromosuccinimide. It is useful in the protection of glutamine and asparagine residues in peptide synthesis, reagent for the N-</p>Formula:C15H16O3Purity:98+%Color and Shape:White, PowderMolecular weight:244.294,4'-DIMETHOXYBENZHYDROL
CAS:Formula:C15H16O3Purity:98%Color and Shape:SolidMolecular weight:244.28574,4'-Dimethoxybenzhydrol
CAS:<p>4,4'-Dimethoxybenzhydrol is a reaction system that has been used to control experiments in which the nucleophile is an iron catalyst. The reaction system was also used to determine the reactivity of various functional groups. The linear plot of the rate of reaction versus concentration of cyclopentenes, hydroxyl group, and dehydrated functionalities indicated that these factors had little effect on the rate of reaction. However, it was found that lactams and trifluorides were able to increase the rate of reaction. Anilines were also found to be effective as they reacted with hydrogen peroxide to form phenoxides.</p>Formula:C15H16O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:244.29 g/mol4,4'-Dimethoxybenzhydrol
CAS:Controlled Product<p>Applications 4,4'-Dimethoxybenzhydrol acts as a reagent in the preparation of aryloxyacetamide derivatives and their biological activity as neuroprotective agents. Preparation and anticancer activity of quebecol and analogs.<br>References Zhong, Y., et al.: Bioorg. Med. Chem. Lett., 26, 2526 (2016); Pericherla, K., et al.: Bioorg. Med. Chem. Lett., 23, 5329 (2013)<br></p>Formula:C15H16O3Color and Shape:NeatMolecular weight:244.29
