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1314217-69-0

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  • 7-methyl-5-[(3-piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl]-2-[4-(trifluoromethoxy)benzyl]-2,3-dihydro-1H-isoindol-1-one methanesulphonate

    Cas No: 1314217-69-0

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1314217-69-0 Usage

General Description

7-methyl-5-[(3-piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl]-2-[4-(trifluoromethoxy)benzyl]-2,3-dihydro-1H-isoindol-1-one methanesulphonate is a chemical compound that is used in research and pharmaceuticals. It is a methanesulphonate salt form of a compound that contains a heterocyclic structure with a piperazine moiety, oxadiazole ring, and a benzyl group with a trifluoromethoxy substituent. 7-methyl-5-[(3-piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl]-2-[4-(trifluoromethoxy)benzyl]-2,3-dihydro-1H-isoindol-1-one methanesulphonate may have potential bioactive properties and could be used for various applications, including drug development and medical research. Its specific biological activities and mechanisms of action may vary depending on the context and the specific use in which it is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 1314217-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,2,1 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1314217-69:
(9*1)+(8*3)+(7*1)+(6*4)+(5*2)+(4*1)+(3*7)+(2*6)+(1*9)=120
120 % 10 = 0
So 1314217-69-0 is a valid CAS Registry Number.

1314217-69-0Downstream Products

1314217-69-0Relevant articles and documents

Isoindolone formation via intramolecular Diels-Alder reaction

Ball, Matthew,Boyd, Alistair,Churchill, Gwydion,Cuthbert, Murray,Drew, Mark,Fielding, Mark,Ford, Gair,Frodsham, Lianne,Golden, Michael,Leslie, Kevin,Lyons, Sarah,McKeever-Abbas, Ben,Stark, Andrew,Tomlin, Paula,Gottschling, Stephen,Hajar, Abraham,Jiang, Ji-Long,Lo, Josephine,Suchozak, Bob

, p. 741 - 747 (2012/07/31)

The intramolecular Diels-Alder reaction provides a useful synthetic methodology to build biologically active and synthetically useful isoindolone ring systems. An application of this methodology, providing an efficient manufacturing route to an mGluR2 positive allosteric modulator via a 1,5,7-substituted isoindolone, is reported herein.

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