Cas 1238398-79-2,3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole

1238398-79-2

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Product Name: 3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole
Synonyms: 3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole
CAS NO:1238398-79-2
Molecular Formula:
Molecular Weight: 646.783
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: 3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole(1238398-79-2)
EPA Substance Registry System: 3-(4,6-Dimethoxy-3-methyl-1H-indol-2-yl)-6,8-dimethoxy-1,3-bis-(4-methoxy-phenyl)-1,9-dimethyl-2,3-dihydro-1H-pyrrolo[1,2-a]indole(1238398-79-2)

Safety Data

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Safety Statements: N/A
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Hazardous Substances Data: 1238398-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1238398-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,8,3,9 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1238398-79:
(9*1)+(8*2)+(7*3)+(6*8)+(5*3)+(4*9)+(3*8)+(2*7)+(1*9)=192
192 % 10 = 2
So 1238398-79-2 is a valid CAS Registry Number.

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1238398-79-2Relevant academic research and scientific papers

Acid-catalyzed reactions of 3-substituted-4,6-dimethoxyindoles with ketones

Wood, Kasey,Black, David StC.,Kumar, Naresh

experimental part, p. 761 - 770 (2011/08/03)

Activated 3-substituted-4,6-dimethoxyindoles undergo acid catalyzed condensation with acetone and acetophenones in the presence of hydrochloric acid to give pyrrolo[a]indoles. Mixed pyrrolo[a]indoles can similarly be formed using a 1:1 mixture of two indo

Acid-catalysed reaction of activated indoles with methyl ketones

Black, David St C.,Craig, Donald C.,Kumar, Naresh

, p. 1587 - 1590 (2007/10/02)

4,6-Dimethoxy-3-methylindole can be converted by treatment with acetone or acetophenones in methanolic hydrochloric acid into ring-fused indoles in good yields.

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