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1,4-Naphthalenedione, 2,3-dihydro-2-hydroxy-2-(phenylmethyl)-, also known as 2-hydroxy-2-(phenylmethyl)-2,3-dihydro-1,4-naphthalenedione, is a chemical compound with the molecular formula C15H12O3. It is a derivative of 1,4-naphthoquinone, featuring a hydroxyl group and a benzyl group attached to the 2-position of the molecule. 1,4-Naphthalenedione, 2,3-dihydro-2-hydroxy-2-(phenylmethyl)- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and dyes, particularly those involving the naphthalene core structure. The compound's chemical properties and reactivity are influenced by the presence of the hydroxyl and benzyl groups, which can participate in various chemical reactions, such as esterification, oxidation, and reduction.

63534-46-3

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63534-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63534-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63534-46:
(7*6)+(6*3)+(5*5)+(4*3)+(3*4)+(2*4)+(1*6)=123
123 % 10 = 3
So 63534-46-3 is a valid CAS Registry Number.

63534-46-3Downstream Products

63534-46-3Relevant academic research and scientific papers

PHOTOCHEMICAL REACTION OF EPOXYNAPHTOQUINONE WITH AMINE. ITS DEPENDENCY ON SOLVENT STUDIED BY CIDNP TECHNIQUE

Maruyama, Kazuhiro,Otsuki, Tetsuo,Osuka, Atsuhiro,Suzuki, Hitomi

, p. 1 - 4 (2007/10/02)

The oxirane ring of epoxynaphthoquinones was reductively opened upon irradiation in the presence of triethylamine and, in addition, a cross adduct was obtained in the reaction with N,N-dimethylaniline in benzene.CIDNP signals observed in the reaction with N,N-dimethylaniline were interpreted as evidence for hydrogen atom abstraction in benzene and for electron transfer in acetone and acetonitrile.

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