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2-(diphenylmethyl)naphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14039-65-7

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14039-65-7 Usage

Physical appearance

Yellow crystalline solid

Main uses

a. Intermediate in the production of synthetic resins and dyes
b. Stabilizer in plastic materials
c. Intermediate in the synthesis of pharmaceuticals

Potential applications

Organic synthesis and materials science

Chemical structure and reactivity

Unique

Handling precautions

May pose health and environmental hazards if not managed properly

Check Digit Verification of cas no

The CAS Registry Mumber 14039-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,3 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14039-65:
(7*1)+(6*4)+(5*0)+(4*3)+(3*9)+(2*6)+(1*5)=87
87 % 10 = 7
So 14039-65-7 is a valid CAS Registry Number.

14039-65-7Relevant academic research and scientific papers

Enantioselective epoxidation of 2-substituted 1,4-naphthoquinones using gem-dihydroperoxides

Bunge, Alexander,Hamann, Hans-Jürgen,McCalmont, Eve,Liebscher, Jürgen

supporting information; experimental part, p. 4629 - 4632 (2009/10/26)

New gem-dihydroperoxides were successfully used for DBU-promoted enantioselective epoxidation of 2-substituted 1,4-naphthoquinones. The corresponding 1,4-naphthoquinone epoxides were obtained in yields up to 97% and ee's up to 82%.

Thermal Decomposition of Homoquinones

Oshima, Takumi,Tamada, Kazushi,Nagai, Toshikazu

, p. 3325 - 3334 (2007/10/02)

Thermolysis of diphenyl- and biphenyl-2,2'-diyl-substituted homobenzoquinones 1 and homonaphthoquinones 2 with substituents X3 (= Me, Cl, Br) has been investigated at 100 deg C.The biphenyl-2,2'-diylhomoquinones 1 and 2 bearing halogeno substit

Catalytic Asymmetric Induction in Oxidation Reactions. Synthesis of Optically Active Epoxynaphthoquinones

Pluim, Henk,Wynberg, Hans

, p. 2498 - 2502 (2007/10/02)

Optically active 2,3-epoxides of a variety of substituted 1,4-naphthoquinones have been prepared in an asymmetric synthesis.Enantiomeric excess of up to 45percent were realized.Some data could be obtained concerning the influence of substituents on the en

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