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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 is a complex organic chemical compound that features a heterocyclic structure. It incorporates a piperazine moiety, an oxadiazole ring, and a benzyl group substituted with a trifluoromethoxy group. 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 typically found in its methanesulphonate salt form and is utilized in research and pharmaceutical applications due to its potential bioactive properties.

1314217-69-0

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1314217-69-0 Usage

Uses

Used in Pharmaceutical Research:
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 serves as a valuable component in pharmaceutical research. Its unique structure and potential bioactivity make it a candidate for the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Drug Development:
In the field of drug development, 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 be employed as a lead molecule or a structural component in the design of novel therapeutic agents. Its heterocyclic nature and functional groups could be leveraged to create drugs with specific mechanisms of action, potentially leading to treatments for various diseases and conditions.
Used in Medical Research:
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 also has applications in medical research, where it can be used to study biological processes and the effects of different chemical modifications on its activity. This can contribute to a better understanding of disease mechanisms and the discovery of new therapeutic targets.
Note: The specific applications and uses mentioned are hypothetical and based on the general properties of similar compounds. The actual uses of 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 would depend on its demonstrated bioactivity, safety, and efficacy in relevant biological assays and clinical trials.

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 academic research and scientific papers

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.

PROCESS FOR MAKING A METABOTROPIC GLUTAMATE RECEPTOR POSITIVE ALLOSTERIC MODULATOR - 874

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, (2011/08/03)

Processes for making 7-methyl-5-(3piperazin-1-ylmethyl-[1,2,4]oxadiazol-5-yl)-2-(4- trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one

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