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2-Isopropylnaphtho[2,3-b]furan-4,9-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13019-43-7

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13019-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13019-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,1 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13019-43:
(7*1)+(6*3)+(5*0)+(4*1)+(3*9)+(2*4)+(1*3)=67
67 % 10 = 7
So 13019-43-7 is a valid CAS Registry Number.

13019-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-ylbenzo[f][1]benzofuran-4,9-dione

1.2 Other means of identification

Product number -
Other names -

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:13019-43-7 SDS

13019-43-7Relevant academic research and scientific papers

A Complete and Unambiguous 1H and 13C NMR Signals Assignment of para?Naphthoquinones, ortho- And para-Furanonaphthoquinones

Borgati, Tatiane F.,de Souza Filho, José D.,de Oliveira, Alaíde B.

, p. 1138 - 1149 (2019/08/26)

A complete and unambiguous assignment of 1H and 13C nuclear magnetic resonance (NMR) signals of 29 naphthoquinones is reported on the basis of one- and two-dimensional NMR techniques (1H, 13C, 1H-sup

Method for synthesizing coumarone naphthoquinone derivative

-

Paragraph 0070; 0074; 0075; 0076, (2016/10/08)

The invention discloses a method for synthesizing a coumarone naphthoquinone derivative. The method comprises the following steps that 2-hydroxyl-3-substituted ethylene-1,4-naphthoquinone is used as raw materials, and the angular coumarone naphthoquinone derivative is synthesized in an organic solvent under the effect of iodine; or the 2-hydroxyl-3-substituted ethylene-1,4-naphthoquinone is used as raw materials, the angular coumarone naphthoquinone derivative is firstly synthesized in an organic solvent under the effect of the iodine, and then, the angular coumarone naphthoquinone derivative is used for synthesizing the straight coumarone naphthoquinone derivative under the acid condition. The method has the advantages that the experiment steps are few; the operation is simple; the selectivity is high; the yield is high; a higher application value is realized.

The iodine-mediated highly regioselective synthesis of angular and linear naphthofuroquinones

Liu, Suyou,Long, Lijun,Xie, Duoduo,Liu, Lijun,Ma, Dayou

supporting information, p. 6730 - 6733 (2018/05/14)

Naphthofuroquinones are of great value in medicinal chemistry. In this letter, a facile method for highly regioselective synthesis of both linear and angular naphthofuroquinones has been developed via iodine mediated cyclization of 2-hydroxy-3-substituted

Selenium reagent in the synthesis of naphtho[2,3-b]furan-4,9-diones

De Oliveira, Alaide Braga,Raslan, Delio Soares,Khuong-Huu, Francoise

, p. 6873 - 6876 (2007/10/02)

Phenylselenoetherification was used to synthezise naphtho[2,3-b]furan-4,9-diones and naphtho[2,3-b]pyran-5,10-diones from 2-hydroxynaphthoquinones.

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