Cas 96567-24-7,Pyrrolo[2,1-a]isoquinoline-2-carboxylic acid, 1-[[[2-(3,4-dimethoxyphenyl)ethyl]amino]methyl]-5,6-dihydro-8,9-dimeth oxy-, ethyl ester

96567-24-7

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Basic information

Product Name: Pyrrolo[2,1-a]isoquinoline-2-carboxylic acid, 1-[[[2-(3,4-dimethoxyphenyl)ethyl]amino]methyl]-5,6-dihydro-8,9-dimeth oxy-, ethyl ester
Synonyms:
CAS NO:96567-24-7
Molecular Formula: C28H34N2O6
Molecular Weight: 494.588
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: Pyrrolo[2,1-a]isoquinoline-2-carboxylic acid, 1-[[[2-(3,4-dimethoxyphenyl)ethyl]amino]methyl]-5,6-dihydro-8,9-dimeth oxy-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Pyrrolo[2,1-a]isoquinoline-2-carboxylic acid, 1-[[[2-(3,4-dimethoxyphenyl)ethyl]amino]methyl]-5,6-dihydro-8,9-dimeth oxy-, ethyl ester(96567-24-7)
EPA Substance Registry System: Pyrrolo[2,1-a]isoquinoline-2-carboxylic acid, 1-[[[2-(3,4-dimethoxyphenyl)ethyl]amino]methyl]-5,6-dihydro-8,9-dimeth oxy-, ethyl ester(96567-24-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 96567-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96567-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96567-24:
(7*9)+(6*6)+(5*5)+(4*6)+(3*7)+(2*2)+(1*4)=177
177 % 10 = 7
So 96567-24-7 is a valid CAS Registry Number.

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96567-24-7Relevant academic research and scientific papers

3,4-Dihydroisoquinolines, I. 5,6-Dihydropyrroloisoquinolines via Rearrangement of 1-(3-Furyl)-3,4-dihydroisoquinolines

Loesel, Walter,Daniel, Helmut

, p. 413 - 427 (2007/10/02)

A new synthesis of 5,6-dihydropyrroloisoquinolines 2 via base-catalysed ring transformation of 1-(3-furyl)-3,4-dihydroisoquinolines 1 has been developed.The structure of 2 was derived from spectroscopic data and reaction products.A pathway for the

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