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(1-hydroxynaphthalen-2-yl)(2-iodophenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

289911-20-2

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289911-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 289911-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,9,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 289911-20:
(8*2)+(7*8)+(6*9)+(5*9)+(4*1)+(3*1)+(2*2)+(1*0)=182
182 % 10 = 2
So 289911-20-2 is a valid CAS Registry Number.

289911-20-2Relevant academic research and scientific papers

An intramolecular arylation route to the kinafluorenones

Qabaja, Ghassan,Jones, Graham B.

, p. 5317 - 5320 (2000)

Intramolecular palladium-mediated arylation approaches to benzo[b]fluorenes have been investigated. The methodology has been applied in a short synthesis of kinafluorenone 2, providing an effective alternative to Friedel-Crafts-based approaches. (C) 2000 Elsevier Science Ltd.

An efficient copper-catalytic system for performing intramolecular O-arylation reactions in aqueous media. New synthesis of xanthones

Barbero, Nekane,Sanmartin, Raul,Dominguez, Esther

supporting information; experimental part, p. 830 - 836 (2010/04/23)

A safe, efficient protocol for the copper-catalysed intramolecular O-arylation of 2-halobenzophenones on water to afford the valuable xanthone framework is reported. The recovery and the successful reutilization of the aqueous solution containing the copp

Annulation strategies for benzo[b]fluorene synthesis: efficient routes to the kinafluorenone and WS-5995 antibiotics.

Qabaja,Jones

, p. 7187 - 7194 (2007/10/03)

Intramolecular palladium-mediated arylation approaches to benzo[b]fluorenes have been investigated. The methodology has been applied in a short synthesis of tri-O-methylkinafluorenone, providing an effective alternative to Friedel-Crafts-based approaches. During the course of this work, an acid-promoted quinolactonization of naphthoquinones was also developed, providing direct access to either ortho or para isomers as desired. Application of this methodology in syntheses of the antibiotics WS-5995A, WS-5995C, and functional analogues was demonstrated, and antitumoral activity of this class was determined.

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