Cas 137304-27-9,(3aS,10aR)-5-Benzoyl-2-{4-[4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,5,10,10a-tetrahydro-3aH-pyrrolo[3,4-b]carbazole-1,3-dione

137304-27-9

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Product Name: (3aS,10aR)-5-Benzoyl-2-{4-[4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,5,10,10a-tetrahydro-3aH-pyrrolo[3,4-b]carbazole-1,3-dione
Synonyms:
CAS NO:137304-27-9
Molecular Formula:
Molecular Weight: 605.649
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: (3aS,10aR)-5-Benzoyl-2-{4-[4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,5,10,10a-tetrahydro-3aH-pyrrolo[3,4-b]carbazole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,10aR)-5-Benzoyl-2-{4-[4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,5,10,10a-tetrahydro-3aH-pyrrolo[3,4-b]carbazole-1,3-dione(137304-27-9)
EPA Substance Registry System: (3aS,10aR)-5-Benzoyl-2-{4-[4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzyl]-phenyl}-4,5,10,10a-tetrahydro-3aH-pyrrolo[3,4-b]carbazole-1,3-dione(137304-27-9)

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Hazardous Substances Data: 137304-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137304-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 137304-27:
(8*1)+(7*3)+(6*7)+(5*3)+(4*0)+(3*4)+(2*2)+(1*7)=109
109 % 10 = 9
So 137304-27-9 is a valid CAS Registry Number.

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137304-27-9Relevant academic research and scientific papers

DIELS-ALDER REACTIONS UNDER MOLECULAR SIEVE CATALYSIS: ENHANCEMENT OF REACTIVITY IN CYCLIZATION REACTIONS WITH N-BENZOYLINDOLE-2,3-QUINODIMETHANE TO FUNCTIONALIZED CARBAZOLES

Pindur, Ulf,Haber, Manfred

, p. 1463 - 1470 (2007/10/02)

In the presence of highly activated molecular sieves (4 Angstroem), the Diels-Alder reactivity of in situ generated N-benzoylindole-2,3-quinomethane is enhanced considerably.Reactions of this species with a variety of carbodienophiles give rise to novel f

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