Cas 106462-66-2,1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride

106462-66-2

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Basic information

Product Name: 1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride
Synonyms:
CAS NO:106462-66-2
Molecular Formula:
Molecular Weight: 393.911
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(106462-66-2)
EPA Substance Registry System: 1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(106462-66-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 106462-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106462-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,6 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106462-66:
(8*1)+(7*0)+(6*6)+(5*4)+(4*6)+(3*2)+(2*6)+(1*6)=112
112 % 10 = 2
So 106462-66-2 is a valid CAS Registry Number.

106462-66-2Upstream product

106462-56-0 1-(3,4-Dimethoxy-benzyl)-5,8-dimethoxy-2-methyl-3,4-dihydro-isoquinolinium; iodide

106462-66-2Downstream Products

106462-66-2Relevant academic research and scientific papers

A Novel Ring Closure leading to 3,9-Dihydroxyaporphines (3,9-Dihydroxy-4H-dibenzoquinolines). Part 2

Copp, Frederick C.,Franzmann, Karl W.,Grundy, Julian,Whalley, W. Basil

, p. 2455 - 2462 (2007/10/02)

3,9-Dihydroxyaporphines are formed by a novel and efficient ring closure when certain 1-benzyl-1,2,3,4-tetrahydro-5,8-dimethoxyisoquinolines are demethylated in refluxing hydrobromic acid.In accordance with a mechanism proposed in Part 1, it has been show

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