Cas 441283-66-5,1-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one

441283-66-5

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Basic information

Product Name: 1-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one
Synonyms: 1-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one
CAS NO:441283-66-5
Molecular Formula:
Molecular Weight: 469.586
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-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one(441283-66-5)
EPA Substance Registry System: 1-benzyl-4-(1-cyclopent-2-enyl-1H-indol-3-yl)-3-(1H-indol-3-yl)-1,5-dihydro-pyrrol-2-one(441283-66-5)

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: 441283-66-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 441283-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,2,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 441283-66:
(8*4)+(7*4)+(6*1)+(5*2)+(4*8)+(3*3)+(2*6)+(1*6)=135
135 % 10 = 5
So 441283-66-5 is a valid CAS Registry Number.

441283-66-5Upstream product

441283-66-5Downstream Products

441283-66-5Relevant academic research and scientific papers

Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons.

Trost, Barry M,Krische, Michael J,Berl, Volker,Grenzer, Ellen M

, p. 2005 - 2008 (2002)

[reaction: see text] Monosubstituted isomerically pure indolopyrrolocarbazole precursors have been prepared via palladium-catalyzed asymmetric allylic alkylation methodology, employing both achiral cyclopentenyl electrophiles and chiral glycal derivatives

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