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α-(p-methyoxyphenyl)malonmorpholide is a complex organic chemical compound with the molecular formula C20H21NO4. It is a derivative of morpholide, which is a morphine analog with potent analgesic properties. The compound features a p-methyloxyphenyl group attached to the alpha position of the malonmorpholide structure, which contributes to its pharmacological activity. This specific chemical modification may alter the binding affinity and selectivity of the compound at opioid receptors, potentially enhancing its therapeutic effects or reducing side effects compared to other opioids. The compound is of interest in medicinal chemistry for its potential applications in pain management and as a research tool to understand the mechanisms of opioid action.

79815-72-8

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79815-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79815-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79815-72:
(7*7)+(6*9)+(5*8)+(4*1)+(3*5)+(2*7)+(1*2)=178
178 % 10 = 8
So 79815-72-8 is a valid CAS Registry Number.

79815-72-8Downstream Products

79815-72-8Relevant academic research and scientific papers

Studies on Paraionic Compounds. Anhydro-1-hydroxy-3-oxopyrazolopyrazolium Hydroxides. Formation and Stability of a Novel Series of 4n? Heterocyclic Betaines.

Zvilichovsky, Gury,David, Mordechai

, p. 295 - 300 (2007/10/02)

Different substituted anhydro-1-hydroxy-3-oxopyrazolopyrazolium hydroxides were prepared by the reaction of 1,3-dicarbonyl compounds with derivatives of 4-phenyl-3,5-dihydroxypyrazole.These diazapentalene derivatives belong to new series of 4n? cyclic betaines which are named "paraionic" heterocycles.The effects of substituents on the stability of both the anionic and the cationic rings were kinetically studied.Selective cleavage of either the anionic or the cationic ring was achieved by varying the conditions of the reaction with morpholine.Electron releasing groups on the cationic ring and electron attracting groups on the anionic ring enhance the stability of the bicyclic system.They also cause a hypsochromic shift of the visible light absorption.

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