Cas 926291-40-9,[1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester

926291-40-9

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Basic information

Product Name: [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester
Synonyms: [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester
CAS NO:926291-40-9
Molecular Formula:
Molecular Weight: 455.308
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-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester(926291-40-9)
EPA Substance Registry System: [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester(926291-40-9)

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: 926291-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 926291-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,2,9 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 926291-40:
(8*9)+(7*2)+(6*6)+(5*2)+(4*9)+(3*1)+(2*4)+(1*0)=179
179 % 10 = 9
So 926291-40-9 is a valid CAS Registry Number.

926291-40-9Upstream product

926291-40-9Downstream Products

926291-42-1 {1-[1-benzyl-4-(2,3-dihydro-1H-indol-1-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]-1H-indol-3-yl}acetic acid methyl ester

926291-40-9Relevant academic research and scientific papers

Introduction of pharmacophore groups into bis(indol-1-yl)maleimides and 6H-pyrrolo[3,4: 2,3][1,4]diazepino[6,7,1-hi]-indolo-8,10(7H,9H)-diones

Lakatosh,Simonov,Luzikov,Preobrazhenskaya

, p. 435 - 440 (2006)

The synthesis of bis(indol-1-yl)maleimides and polycondensed [1,4]diazepines containing various functional groups, which are the analogs of biologically active indolo[2,3-a]carbazoles, is described. Functional groups were introduced directly into [1,4]dia

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