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1,4-Ethenonaphtho[2,3-d][1,2]dioxin, also known as 1,4-dihydro-1,4-dimethyl-5,10-diphenyl-, is a complex organic compound with a unique molecular structure. It belongs to the class of naphtho derivatives, which are characterized by the presence of a naphthalene ring system fused with a dioxin ring. This particular compound features a 1,4-ethenonaphtho core, with a 1,2-dioxin ring attached to it. The molecule also includes two methyl groups attached to the 1,4-dihydro positions and two phenyl groups at the 5,10 positions, which contribute to its stability and reactivity. Due to its complex structure, 1,4-Ethenonaphtho[2,3-d][1,2]dioxin, 1,4-dihydro-1,4-dimethyl-5,10-diphenyl- has potential applications in various chemical and pharmaceutical industries, although its specific uses and properties would require further investigation and research.

20153-17-7

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20153-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20153-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,5 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20153-17:
(7*2)+(6*0)+(5*1)+(4*5)+(3*3)+(2*1)+(1*7)=57
57 % 10 = 7
So 20153-17-7 is a valid CAS Registry Number.

20153-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethyl-9,10-diphenylanthracene 1,4-endoperoxide

1.2 Other means of identification

Product number -
Other names 1,4-dimethyl-9,10-diphenyl-1,4-dihydro-1,4-epidioxido-anthracene

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:20153-17-7 SDS

20153-17-7Relevant academic research and scientific papers

Transformations photochimiques d'endoperoxydes derives d'hydrocarbures aromatiques polycycliques IV. Effet de phenyles en peri sur la photo-isomerisation des endoperoxydes-1,4 tetrahydroaromatiques

Rigaudy, Jean,Caspar, Alain,Baranne-Lafont, Joele,Chassagnard, Claude

, p. 195 - 200 (2007/10/02)

Photolysis in benzene at long wavelengths of 1,4-epidioxy-1,4-dimethyl-9,10-diphenyl-1,2,3,4-tetrahydroanthracene 1a affords essentially two products: 2,5-epoxy-2,5-dimethyl-6,11-diphenyl-2,3,4,5-tetrahydronaphthooxepine 8a and 5a,8-dimethyl-9-phen

PHOTO-OXYGENATIONS DE COMPOSES AROMATIQUES SENSIBILISEES PAR DES ACCEPTEURS D'ELECTRON

Santamaria, Jean

, p. 4511 - 4514 (2007/10/02)

Photo-oxygenation of aromatic compounds sensitized by electron acceptors, like 9-10 dicyanoanthracene (DCA) is shown to proceed by two distinct mechanism each one beginning by an electron-transfer step : in the first way superoxide ion is involve

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