Cas 34132-41-7,1H-1-Benzazepine-3,4-dicarboxylic acid, 2,3-dihydro-1-methyl-2-(1-methyl-1H-indol-3-yl)-, dimethyl ester

34132-41-7

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Basic information

Product Name: 1H-1-Benzazepine-3,4-dicarboxylic acid, 2,3-dihydro-1-methyl-2-(1-methyl-1H-indol-3-yl)-, dimethyl ester
Synonyms:
CAS NO:34132-41-7
Molecular Formula: C24H24N2O4
Molecular Weight:
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: 1H-1-Benzazepine-3,4-dicarboxylic acid, 2,3-dihydro-1-methyl-2-(1-methyl-1H-indol-3-yl)-, dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-1-Benzazepine-3,4-dicarboxylic acid, 2,3-dihydro-1-methyl-2-(1-methyl-1H-indol-3-yl)-, dimethyl ester(34132-41-7)
EPA Substance Registry System: 1H-1-Benzazepine-3,4-dicarboxylic acid, 2,3-dihydro-1-methyl-2-(1-methyl-1H-indol-3-yl)-, dimethyl ester(34132-41-7)

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: 34132-41-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 34132-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34132-41:
(7*3)+(6*4)+(5*1)+(4*3)+(3*2)+(2*4)+(1*1)=77
77 % 10 = 7
So 34132-41-7 is a valid CAS Registry Number.

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34132-41-7Relevant academic research and scientific papers

Photocycloaddition of Dimethyl Acetylenedicarboxylate to Activated Indoles

Davis, Paul D.,Neckers, Douglas C.

, p. 456 - 462 (2007/10/02)

Photocycloaddition reactions of N-methylindoles to dimethyl acetylenedicarboxylate (DMAD) yield derivatives of cyclobutenes: 9,10-bis(methoxycarbonyl)-2-methyl-3,4-benzo-2-azatricyclodeca-3,9-dienes.No secondary photorearrangements are prevalent, but ring opening of the formed cyclobutenes is effected at moderate temperatures.

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