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N,O-dimethyl-N-norarmepavine methyliodide is a chemical compound with the molecular formula C18H26IN2O. It is a derivative of norarmepavine, a synthetic opioid analgesic, and is characterized by the presence of a methyl group attached to the nitrogen atom and an iodide ion. N,O-dimethyl-N-norarmepavine methyliodide is primarily used in scientific research and pharmaceutical development, particularly in the study of opioid receptors and their interactions. Its chemical structure and properties make it a valuable tool for understanding the mechanisms of opioid action and potentially developing new therapeutic agents for pain management.

7630-50-4

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7630-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7630-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7630-50:
(6*7)+(5*6)+(4*3)+(3*0)+(2*5)+(1*0)=94
94 % 10 = 4
So 7630-50-4 is a valid CAS Registry Number.

7630-50-4Downstream Products

7630-50-4Relevant academic research and scientific papers

Luxandrine, a quaternary benzylisoquinoline from Pseudoxandra sclerocarpa

Cortes, Diego,Wannigama, G.Percy,Saez, Jairo,Cave, Andre

, p. 2693 - 2695 (1986)

A new 6,7-dihydroxytetrahydrobenzylisoquinoline has been isolated and identified from the quaternary alkaloidal fraction of the bases of Pseudoxandra sclerocarpa.

Effect of isoquinoline alkaloids of different structural types on antiplatelet aggregation in vitro

Chia, Yi-Chen,Chang, Fang-Rong,Wu, Chin-Chung,Teng, Che-Ming,Chen, Keh-Shaw,Wu, Yang-Chang

, p. 1238 - 1241 (2007/10/03)

Forty-one isoquinoline alkaloids were tested for antiplatelet aggregation effects. Among them, (-)-discretamine (6), protopine (7), ochotensimine (18), O-methylarmepavinemethine (23), lindoldhamine (25), isotetrandrine (26), thalicarpine (27), papaverine (28), and D-(+)-N-norarmepavine (32) exhibited significant inhibitory activity towards adenosine 5′-diphosphate (ADP)-, arachidonic acid (AA)-, collagen-, and/or platelet-activating factor (PAF)-induced platelet aggregation. The results are discussed on the basis of structure-activity relationships. Georg Thieme Verlag KG Stuttgart.

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