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4-(3,4-dimethoxybenzyl)-6,7-dimethoxyisoquinoline is a complex organic compound belonging to the isoquinoline family. It is characterized by a central isoquinoline ring system, which is a tricyclic structure with two benzene rings fused to a pyridine ring. The compound features three methoxy groups at positions 6, 7, and 4, with the latter being attached to a benzyl group that itself has two methoxy groups at positions 3 and 4. This specific arrangement of functional groups endows the molecule with unique chemical and biological properties, making it a subject of interest in various fields, including medicinal chemistry and materials science.

32871-93-5

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32871-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32871-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32871-93:
(7*3)+(6*2)+(5*8)+(4*7)+(3*1)+(2*9)+(1*3)=125
125 % 10 = 5
So 32871-93-5 is a valid CAS Registry Number.

32871-93-5Relevant academic research and scientific papers

BIOTRANSFORMATION OF ISOPAPAVERINE BY SILENE ALBA CELL SUSPENSIONS

Christinaki, Helene,Bister-Miel, Francoise,Hammoumi, Abderahmane,Bury, Michele,Guignard, Jean-Louis,Viel, Claude

, p. 2991 - 2994 (2007/10/02)

Key Word Index-Silene alba; Caryophyllaceae; cell suspensions; isopapaverine; 4-benzyl isoquinolines; biotransformations; syntheses; structural analysis. Silene alba cell suspension was supplied with isopapaverine (methanesulphonate), a papaverine analogu

New structural analogs of papaverine: 3 benzyl 6,7 dimethoxy (di and tetrahydro) isoquinolines

Prudhommeaux,Ernouf,Foussard Blanpin,Viel

, p. 19 - 28 (2007/10/04)

Syntheses of 3 benzyl 3,4 dihydroisoquinolines by cyclisation of a N acyl α benzylhomoveratrylamine by means of polyphosphoric acid ester, in boiling toluene, gave yields between 60 and 90%. While the hydrogenation of these dihydroisoquinolines to tetrahydroisoquinolines with an alkaline borohydride gave satisfactory result, their dehydrogenation into isoquinolines could not be accomplished. Pharmacological properties of the hydrobromides or hydrochlorides of the bases of the two series of the aforementioned 3 benzylisoquinolines and comparison of their activities with those of papaverine and the analogues 1 and 4 benzylisoquinolines are reported.

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