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7-(3-Piperidinylmethyloxy)-2H-chromen-2-one is a chemical compound with the molecular formula C16H17NO3. It is a derivative of chromone, a type of organic compound characterized by a benzopyran structure. This specific compound features a 7-piperidinylmethoxy substituent, which is a piperidine ring attached to a methoxy group. The presence of this functional group may influence the compound's reactivity and properties, potentially affecting its use in various applications, such as in pharmaceuticals or as a chemical intermediate. The compound's structure and properties make it a subject of interest for researchers in organic chemistry and related fields.

946724-98-7

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946724-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 946724-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,7,2 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 946724-98:
(8*9)+(7*4)+(6*6)+(5*7)+(4*2)+(3*4)+(2*9)+(1*8)=217
217 % 10 = 7
So 946724-98-7 is a valid CAS Registry Number.

946724-98-7Downstream Products

946724-98-7Relevant academic research and scientific papers

Investigating alkyl nitrates as nitric oxide releasing precursors of multitarget acetylcholinesterase-monoamine oxidase B inhibitors

Pisani, Leonardo,Iacobazzi, Rosa Maria,Catto, Marco,Rullo, Mariagrazia,Farina, Roberta,Denora, Nunzio,Cellamare, Saverio,Altomare, Cosimo Damiano

, p. 292 - 309 (2019)

Herein we envisaged the possibility of exploiting alkyl nitrates as precursors of alcohol-bearing dual inhibitors targeting acetylcholinesterase (AChE) and monoamine oxidase B (MAO B), key enzymes in neurodegenerative syndromes such as Alzheimer's disease (AD), through biotransformation unmasking an alcoholic function upon nitric oxide (NO) release. The cooperation to neuroprotection of low fluxes of NO and target enzymes’ inhibition by the alcohol metabolites might return a multitargeting effect. The in vitro screening towards ChEs and MAOs of a collection of 21 primary alcohols disclosed a subset of dual inhibitors, among which three diverse chemotypes were selected to study the corresponding nitrates. Nitrate 14 proved to be a brain permeant, potent AChE-MAO B inhibitor by itself. Moreover, it protected human SH-SY5Y lines against rotenone and hydrogen peroxide with a poor inherent cytotoxicity and showed a slow conversion profile to its alcohol metabolite 9d that still behaved as bimodal and neuroprotective molecule.

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