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3-(3,4-dimethoxybenzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20232-49-9

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20232-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20232-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,3 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20232-49:
(7*2)+(6*0)+(5*2)+(4*3)+(3*2)+(2*4)+(1*9)=59
59 % 10 = 9
So 20232-49-9 is a valid CAS Registry Number.

20232-49-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinoline

1.2 Other means of identification

Product number -
Other names 3-(3,4-dimethoxybenzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20232-49-9 SDS

20232-49-9Relevant academic research and scientific papers

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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