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9,10-Anthracenediol, 2-ethyl-9,10-dihydro-, also known as 2-Ethyl-9,10-dihydro-9,10-anthracenediol, is an organic compound with the chemical formula C16H16O2. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and features a dihydroxyl group at the 9,10 positions and an ethyl group at the 2 position. 9,10-Anthracenediol, 2-ethyl-9,10-dihydro- is characterized by its molecular weight of 240.30 g/mol and a melting point of approximately 90-92°C. It is typically used as a chemical intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its complex structure and potential applications, 9,10-Anthracenediol, 2-ethyl-9,10-dihydro- is an important compound in the field of organic chemistry.

2026-28-0

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2026-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2026-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2026-28:
(6*2)+(5*0)+(4*2)+(3*6)+(2*2)+(1*8)=50
50 % 10 = 0
So 2026-28-0 is a valid CAS Registry Number.

2026-28-0SDS

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 2-ethyl-9,10-dihydroanthracene-9,10-diol

1.2 Other means of identification

Product number -
Other names 2-ethyl-9,10-dihydro-9,10-dihydroxyanthracene

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:2026-28-0 SDS

2026-28-0Upstream product

2026-28-0Downstream Products

2026-28-0Relevant academic research and scientific papers

Hydrogenation of 2-ethylanthraquinone with bimetallic monolithic catalysts: An experimental and DFT study

Guo, Yanyan,Dai, Chengna,Lei, Zhigang

, p. 1070 - 1080 (2018)

We studied the hydrogenation of 2-ethylanthraquinone (eAQ) over Pd/SiO2/COR (COR = cordierite) monometallic and Pd-M/SiO2/COR (M = Ni, Fe, Mn, and Cu) bimetallic monolithic catalysts, which were prepared by the co-impregnation method. Detailed investigations showed that the particle sizes and structures of the Pd-M (M = Ni, Fe, Mn, and Cu) bimetallic monolithic catalysts were greatly affected by the second metal M and the mass ratio of Pd to the second metal M. By virtue of the small particle size and the strong interaction between Pd and Ni of Pd-Ni alloy, Pd-Ni bimetallic monolithic catalysts with the mass ratio of Pd/Ni = 2 achieved the highest H2O2 yield (7.5 g/L) and selectivity (95.3%). Moreover, density functional theory calculations were performed for eAQ adsorption to gain a better mechanistic understanding of the molecule-surface interactions between eAQ and the Pd(1 1 1) or PdM(1 1 1) (M = Ni, Fe, Mn, and Cu) surfaces. It was found that the high activity of the bimetallic Pd-Ni catalyst was a result of strong chemisorption between Pd3Ni1 (1 1 1) and the carbonyl group of eAQ.

Photophysical and photochemical processes of 2-methyl, 2-ethyl, and 2-tert-butylanthracenes on silica gel. A substituent effect study

Dabestani, Reza,Higgin, Jashua,Stephenson, Daniel,Ivanov, Ilia N.,Sigman, Michael E.

, p. 10235 - 10241 (2007/10/03)

PAH are organic pollutants formed and released into the environment by the incomplete combustion of fossil fuel, coal, wood, gas, oil, garbage, tobacco, and charbroiled meat. The photophysics and photochemistry of 2-methylanthracene (2MA), 2-ethylanthracene (2EA), and 2-tert-butylanthracene (2TBA) adsorbed on silica were studied at a silica/air interface. 2MA, 2EA, and 2TBA showed no evidence of ground state pairing even at high surface coverages, and crystallized on the surface at higher surface coverages. The photolysis of 2MA, 2EA, and 2TBA at a silica/air interface proceeded more efficiently than the photolysis of anthracene, to produce the corresponding 9,10-endoperoxides formed by the addition of singlet molecular oxygen (type II) to the ground state molecules. At low surface coverages, no evidence of any dimer was observed in photolyzed 2MA, 2EA, and 2TBA samples. A small amount of dimers (isomeric) were observed at higher surface coverages, suggesting that the crystal forms of these molecules may be involved in the dimerization process. The photolysis rate decreased with increasing surface coverage, due to an inner effect induced by crystal formation. Photolysis rate decreased by an order of magnitude in the presence of 1 monolayer of physisorbed water. Time-resolved transient studies of excited triplet states of 2MA, 2EA, and 2TBA showed that triplet lifetimes were shortened on wet silica. The efficiency of singlet molecular oxygen formation significantly decreased on wet silica. These results indicated that decreased photolysis rate was caused by reduced singlet quantum yield in the presence of physisorbed water.

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