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Anthracene,9,9'-methylenebis-, also known as 9,9'-Methylenebis(anthracene) or simply 9,9'-Methylenebisanthracene, is an organic compound with the chemical formula C24H16. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. Anthracene,9,9'-methylenebis- is characterized by its anthracene units connected by a methylene bridge, which gives it unique chemical and physical properties. It is used in various applications, including as a precursor in the synthesis of other organic compounds and as a research chemical in the study of molecular structures and properties. Due to its potential health and environmental risks, it is important to handle this substance with care and in accordance with safety regulations.

15080-14-5

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15080-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15080-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15080-14:
(7*1)+(6*5)+(5*0)+(4*8)+(3*0)+(2*1)+(1*4)=75
75 % 10 = 5
So 15080-14-5 is a valid CAS Registry Number.

15080-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(anthracen-9-ylmethyl)anthracene

1.2 Other means of identification

Product number -
Other names di-9-anthrylmethane

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:15080-14-5 SDS

15080-14-5Downstream Products

15080-14-5Relevant academic research and scientific papers

Charge transfer complex formation between p-chloranil and 1,n-di(9-anthryl)alkanes

Arslan, Mustafa,Masnovi, John

, p. 711 - 716 (2007/10/03)

Dimer model compounds of polyvinylanthracenes (1,n-di(9-anthryl)alkanes, when n = 1-5) were synthesized to model the effects of distance and orientation between anthracene groups in polymeric systems. Charge transfer (CT) complexes of anthracene, 9-methylanthracene and 1,n-di(9-anthryl)alkanes with p-chloranil (p-CHL) have been investigated spectrophotometrically in dichloromethane. The colored products are measured spectrophotometrically at different wavelength depending on the electronic transition between donors and acceptor. The formation constants of the CT complexes were determined by the Benesi-Hildebrand equation. The thermodynamic parameters were calculated by Van't Hoff equation. Stochiometries of the complexes formed between donors and acceptor were defined by the Job's method of the continuous variation and found in 1:1 complexation with donor and acceptor at the maximum absorption bands.

Reaction of 9-α-Chloronaphthylmethylanthracene and Its Homologues with Nucleophiles under Solvolytic Conditions. Effect of the Increase of Bulk at C-α on the Reaction Site

Takagi, Masato,Nojima, Masatomo,Kusabayashi, Shigekazu

, p. 2637 - 2641 (2007/10/02)

The reaction of 9-α-chloronaphthylmethylanthracene and its homologues with (a) sodium ethoxide in ethanol, (b) ethanol in the presence of triethylamine, (c) sodium borohydride in aqueous diglyme, and (d) sodium azide in aqueous NN-dimethylformamide has gi

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