
CAS 13720-08-6
:1,4-Di(Methyl-d3)-naphthalene
Description:
1,4-Di(Methyl-d3)-naphthalene is a deuterated derivative of naphthalene, characterized by the substitution of hydrogen atoms with deuterium in the methyl groups at the 1 and 4 positions of the naphthalene ring. This compound is primarily used in research applications, particularly in studies involving nuclear magnetic resonance (NMR) spectroscopy, where deuterated solvents can enhance spectral resolution and reduce background noise. The presence of deuterium, a stable isotope of hydrogen, allows for the differentiation of signals in NMR experiments. 1,4-Di(Methyl-d3)-naphthalene retains the aromatic properties of naphthalene, exhibiting a planar structure and significant π-electron delocalization, which contributes to its stability and reactivity. It is typically a colorless to pale yellow solid at room temperature and has a relatively low solubility in water but is soluble in organic solvents. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance.
Formula:C12H6D6
Synonyms:- 1,4-Di(Methyl-d3)-naphthalene
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1,4-Di(methyl-d3)-naphthalene
CAS:Controlled Product<p>Applications 1,4-Di(methyl-d3)-naphthalene has been used in the preparation of di(trideuteriomethyl)naphthalene derivatives. 1,4-Di(methyl-d3)-naphthalene is a labeled analogue of 1,4-Dimethylnaphthalene (D476380), a polycyclic aromatic hydrocarbon (PAH) that has been found to retard the development of epidermoid carcinomas in hamster buccal pouch and alter the genes associated with the maintenance of a G1/S phase block possibly through the induction of the cell cycle inhibitors KRP1 and KRP2 in potatoes.<br>References Dizabo, P., et. al.: J. Labelled Compd., 2, 272 (1966); Malament, D.S., Shklar, G.: Carcinogenesis, 2, 723 (1981); Campbell, M.A., et. al.: Fuct. Interg. Genomics, 12, 533 (2012); Andrysik, Z., et. al.: Mutat. Res-Fund. Mol. M., 714, 53 (2011)<br></p>Formula:C12H6D6Color and Shape:NeatMolecular weight:162.26
