25075-81-4 Usage
Uses
Used in Organic Synthesis:
(2 6-NAPHTHALENEDIMETHYLENE)BIS(TRIPHEN& is used as a building block in organic synthesis for creating complex organic molecules. Its unique structure allows for the formation of various chemical bonds and reactions, contributing to the development of new organic compounds.
Used in Material Science:
In the field of material science, (2 6-NAPHTHALENEDIMETHYLENE)BIS(TRIPHEN& is utilized as a component in the development of advanced materials. Its properties, such as increased stability and reactivity, make it suitable for creating materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25075-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25075-81:
(7*2)+(6*5)+(5*0)+(4*7)+(3*5)+(2*8)+(1*1)=104
104 % 10 = 4
So 25075-81-4 is a valid CAS Registry Number.
25075-81-4Relevant academic research and scientific papers
SYNTHESE PHOTOCHIMIQUE D'HYDROCARBURES POLYCYCLIQUES AROMATIQUES ET ETUDE EN RMN-1H DES PROTONS DE BAIE. EFFECTS DE SOLVANT SPECIFIQUES ET EFFECTS NUCLEAIRES OVERHAUSER.
Brison, Jean,Bakker, Claude de,Defay, Nicole,Geerts-Evrard, France,Marchant, Marie-Jeanne,Martin, Richard H.
, p. 901 - 912 (2007/10/02)
"Photochemical synthesis of polycyclic aromatic hydrocarbons and NMR-1H study of bay protons.Specific solvent effects and nuclear Overhauser effects".Dinaphthoanthracene (4a),9-bromo-dinaphthoanthracene (4b), 9-methyldinaphthoanthracene (4c), benzonaphthochrysene (7), benzonaphthoanthracene (3), naphthochrysene (9) and dibenzonaphthochrysene (12) have been synthesized by the photocyclodehydrogenation of 1,2-diarylethylenes (5,8) and bis (arylvinyl)arenes (6,10).The NMR study has been mainly focused on the bay protons involved in specific solvent effects Table 4) and nuclear Overhauser effects (Table 5).