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2-Ethyl-3-methyl-1,4-naphthoquinone is a chemical compound belonging to the class of naphthoquinones, characterized by a fused ring structure consisting of two benzene rings. This specific compound features an ethyl group at the 2-position and a methyl group at the 3-position, both attached to the naphthalene core. It is an organic molecule with the molecular formula C13H12O2, and it exhibits a variety of biological activities, including antioxidant and anti-inflammatory properties. Due to its chemical structure, 2-ethyl-3-methyl-1,4-naphthoquinone is often found in natural products and can be used in the synthesis of various pharmaceuticals and dyes. Its unique properties make it a subject of interest in the fields of chemistry, biology, and medicine.

2589-56-2

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2589-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2589-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2589-56:
(6*2)+(5*5)+(4*8)+(3*9)+(2*5)+(1*6)=112
112 % 10 = 2
So 2589-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-3-9-8(2)12(14)10-6-4-5-7-11(10)13(9)15/h4-7H,3H2,1-2H3

2589-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-3-methylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 3-ethyl-2-methyl-1,4-naphthoquinone

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:2589-56-2 SDS

2589-56-2Downstream Products

2589-56-2Relevant academic research and scientific papers

ELECTRON-TRANSFER PROCESSES: MECHANISMS OF OXIDATION OF ETHERS AND ESTERS BY SILVER-CATALYZED PEROXYDISULPHATE

Minisci, Francesco,Coppa, Fausta,Fontana, Francesca,Zhao, Lihua

, p. 613 - 616 (2007/10/02)

Nucleophilic carbon-centred radicals, generated from the oxidation of diethyl ether, ethyl acetate, propyl acetate, ethyl propionate, diethyl oxalate and 2-phenylethyl acetate by silver-catalyzed decomposition of peroxydisulphate, have been trapped, mostly by naphthoquinone and in a few cases by protonated quinoline. Characterization of the intermediate radicals allows the rationalization of the mechanism of these oxidations, which are likely to occur through an initial electron-transfer step by Ag(II).

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