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9(10H)-Anthracenone, 10-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73653-01-7

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73653-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73653-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73653-01:
(7*7)+(6*3)+(5*6)+(4*5)+(3*3)+(2*0)+(1*1)=127
127 % 10 = 7
So 73653-01-7 is a valid CAS Registry Number.

73653-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-methyl-10H-anthracen-9-one

1.2 Other means of identification

Product number -
Other names 10-Methyl-anthron

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:73653-01-7 SDS

73653-01-7Relevant academic research and scientific papers

Efficient heterogeneous oxidation of alkylarenes with molecular oxygen

Kamata, Keigo,Kasai, Jun,Yamaguchi, Kazuya,Mizuno, Noritaka

, p. 3577 - 3580 (2007/10/03)

(Chemical Equation Presented) Ru(OH)x/Al2O 3 efficiently catalyzes the heterogeneous aerobic oxygenation or oxidative dehydrogenation of alkylarenes to give the corresponding oxygenated or dehydrogenated products. Catalyst/product separation is very easy, and the recovered catalyst is reusable with retention of the high catalytic performance.

Stereoelectronic effects in the deprotonation of arylalkyl radical cations: meso-ethylanthracenes

Tolbert, Laren M.,Khanna, Rajive K.,Popp, Ann E.,Gelbaum, Leslie,Bottomley, Lawrence A.

, p. 2373 - 2378 (2007/10/02)

In contrast to meso-methylanthracenes, which are oxidized by one-electron oxidants to hydroxymethyl derivatives, meso-ethylanthracenes such as 9,10-diethylanthracene (DEA) undergo a facile chemical or biochemical oxidative elimination of ethylene to yield an anthrone. No trace of ethyl side chain oxidation to a 1-hydroxyethyl derivative is observed. The rationale for this dramatic selection between methyl and ethyl reactivity is a stereoelectronic effect on radical cation deprotonation. 9-Ethyl-10-methylanthracene (EMA) undergoes both oxidative pathways, but the competition between the two pathways is mediated by water. This effect is attributed to the intervention of a water cluster in the deprotonation reaction.

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