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7297-72-5

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7297-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7297-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7297-72:
(6*7)+(5*2)+(4*9)+(3*7)+(2*7)+(1*2)=125
125 % 10 = 5
So 7297-72-5 is a valid CAS Registry Number.

7297-72-5Relevant articles and documents

Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions

Hock, Katharina J.,Mertens, Lucas,Metze, Friederike K.,Schmittmann, Clemens,Koenigs, Rene M.

supporting information, p. 905 - 909 (2017/08/14)

Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.

An efficient metal-free pathway to vinyl thioesters with calcium carbide as the acetylene source

Rodygin, Konstantin S.,Ananikov, Valentine P.

supporting information, p. 482 - 486 (2016/01/30)

Chemical reactions involving high-pressure acetylene are not easily performed in a standard laboratory setup. The risk of explosion and technical difficulties drastically complicate the equipment and greatly increase the cost. In this study, we propose th

Asymmetric Intermolecular Pauson-Khand Reactions of Unstrained Olefins: The (o-Dimethylamino)phenylsulfinyl Group as an Efficient Chiral Auxiliary

Rodriguez Rivero, Marta,De La Rosa, Juan Carlos,Carretero, Juan Carlos

, p. 14992 - 14993 (2007/10/03)

The first asymmetric version of intermolecular Pauson?Khand reactions of unstrained alkenes is described. Generally simple acyclic alkenes exhibit low reactivity and regioselectivity in intermolecular Pauson?Khand reactions; however, o-(dimethylamino)phen

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