Cas 1266619-83-3,2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline

1266619-83-3

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Basic information

Product Name: 2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline
Synonyms: 2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline
CAS NO:1266619-83-3
Molecular Formula:
Molecular Weight: 338.452
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: 2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline(1266619-83-3)
EPA Substance Registry System: 2-(2-((1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline(1266619-83-3)

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: 1266619-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1266619-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,6,1 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1266619-83:
(9*1)+(8*2)+(7*6)+(6*6)+(5*6)+(4*1)+(3*9)+(2*8)+(1*3)=183
183 % 10 = 3
So 1266619-83-3 is a valid CAS Registry Number.

1266619-83-3Upstream product

1266619-82-2 2-(2-(di(1H-indol-3-yl)methyl)phenyl)-1,2,3,4-tetrahydroisoquinoline

1266619-83-3Downstream Products

1266619-83-3Relevant academic research and scientific papers

Redox-neutral indole annulation cascades

Haibach, Michael C.,Deb, Indubhusan,De, Chandra Kanta,Seidel, Daniel

scheme or table, p. 2100 - 2103 (2011/04/16)

Aminobenzaldehydes react with indoles in an unprecedented cascade reaction. This acid-catalyzed redox-neutral annulation proceeds via a condensation/1,5-hydride shift/ring-closure sequence. Polycyclic azepinoindoles and related compounds are obtained in a single step with good to excellent yields.

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