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(2 6-NAPHTHALENEDIMETHYLENE)BIS(TRIPHEN& is a chemical compound consisting of two naphthalene rings connected by a dimethylene bridge and attached to three phenyl (triphenyl) groups. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and is known for its unique structure. The presence of triphenyl groups enhances the compound's stability and reactivity in specific chemical reactions. (2 6-NAPHTHALENEDIMETHYLENE)BIS(TRIPHEN& holds potential for various applications in organic synthesis and material science.

25075-81-4

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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.

25075-81-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl-[[6-(triphenylphosphaniumylmethyl)naphthalen-2-yl]methyl]phosphanium,dibromide

1.2 Other means of identification

Product number -
Other names dibromure de 2,6-bis(triphenylphosphoniomethyl)naphtalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25075-81-4 SDS

25075-81-4Downstream Products

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).

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