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2-(methyl-d3)naphthalene is a deuterated analog of 2-methylnaphthalene, a polycyclic aromatic hydrocarbon. 2-(methyl-d3)naphthalene features a naphthalene core with a methyl group (CH3) attached at the 2nd position, where the hydrogen atoms in the methyl group are replaced by deuterium atoms (D). Deuterium is a stable isotope of hydrogen with one proton and one neutron, making it heavier than the common hydrogen isotope. The use of deuterium in 2-(methyl-d3)naphthalene can provide advantages in various applications, such as in chemical reactions, spectroscopy, and as a tracer in biological studies. The deuteration can affect the compound's physical properties, such as boiling point and solubility, and can also influence its chemical reactivity due to the mass difference between hydrogen and deuterium.

2430-39-9

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2430-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2430-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2430-39:
(6*2)+(5*4)+(4*3)+(3*0)+(2*3)+(1*9)=59
59 % 10 = 9
So 2430-39-9 is a valid CAS Registry Number.

2430-39-9Downstream Products

2430-39-9Relevant academic research and scientific papers

Solvent-switched benzylic methylene functionalization: Addition, ring-opening, cyclization, and unexpected cleavage of C-O and C-C bonds

Li, Deng Yuan,Shang, Xue Song,Chen, Guo Rong,Liu, Pei Nian

supporting information, p. 3848 - 3851 (2013/09/02)

Intermolecular benzylic methylene functionalization of exo-cyclic enol ethers has been achieved using imines as reagents and potassium tert-butoxide as the catalyst. Depending on the solvent used, the reaction proceeds by two pathways. In THF, an addition

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