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4-(4-methylphenoxy)-2H-chromen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353259-48-0

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353259-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353259-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,5 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 353259-48:
(8*3)+(7*5)+(6*3)+(5*2)+(4*5)+(3*9)+(2*4)+(1*8)=150
150 % 10 = 0
So 353259-48-0 is a valid CAS Registry Number.

353259-48-0Downstream Products

353259-48-0Relevant academic research and scientific papers

An efficient route to 4-aryloxycoumarins via one-pot reactions of 4-hydroxycoumarins with hypervalent iodine reagents

Gao, Wei,Xu, Linchu,Gong, Chun,Ding, Qiuping,Peng, Yiyuan

supporting information, p. 4020 - 4023 (2017/09/26)

Highly efficient reactions of 4-hydroxycoumarin with hypervalent iodine reagents under mild conditions are described, which give rise to 4-aryloxycoumarins in good to excellent yields.

Pd/Indanone-Based Ligands: An Efficient Catalyst System for Ullmann-Type, Suzuki-Miyaura, and Mizoroki-Heck Cross-Coupling Reactions with Aryl Tosylates and Aryl Halides

Waheed, Mohammed,Ahmed, Naseem

, p. 4372 - 4382 (2017/09/12)

2-Hydroxyindan-1-ones have been efficiently synthesized and successfully applied as ligands in Pd-catalyzed Ullmann type, Suzuki-Miyaura, and Mizoroki-Heck cross-coupling reactions with aryl tosylates and aryl halides. The ligands are air- and moisture-stable and have shown high catalytic activity with Pd(OAc) 2 in these cross-coupling reactions. The system tolerates a variety of functional groups in the product and can be re-used at least three times with maximum efficiency..

Cyclization of 4-Phenoxy-2-coumarins and 2-Pyrones via a Double C-H Activation

Mackey, Katrina,Pardo, Leticia M.,Prendergast, Aisling M.,Nolan, Marie-T.,Bateman, Lorraine M.,McGlacken, Gerard P.

, p. 2540 - 2543 (2016/06/15)

Aryl-heteroaryl coupling via double C-H activation is a powerful transformation that avoids the installation of activating groups. A double C-H activation of privileged biological scaffolds, 2-coumarins and 2-pyrones, is reported. Despite the rich chemistry of these molecular frameworks, the yields are very good. Excellent regioselectivity was achieved on the pyrones. This methodology was applied to the synthesis of flemichapparin C in three steps. Isotope effect experiments were carried out, and a mechanism is proposed.

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