Cas 1104643-81-3,(3aS,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione

1104643-81-3

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Basic information

Product Name: (3aS,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione
Synonyms: (3aS,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione
CAS NO:1104643-81-3
Molecular Formula:
Molecular Weight: 316.359
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,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione(1104643-81-3)
EPA Substance Registry System: (3aS,10bS)-2-phenyl-4,5-dihydropyrrolo[3,4-a]carbazole-1,3(2H,3aH,10H,10bH)-dione(1104643-81-3)

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: 1104643-81-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1104643-81-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,6,4 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1104643-81:
(9*1)+(8*1)+(7*0)+(6*4)+(5*6)+(4*4)+(3*3)+(2*8)+(1*1)=113
113 % 10 = 3
So 1104643-81-3 is a valid CAS Registry Number.

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1104643-81-3Relevant academic research and scientific papers

Organocatalytic asymmetric Diels-Alder reactions of 3-vinylindoles

Gioia, Claudio,Hauville, Agnes,Bernardi, Luca,Fini, Francesco,Ricci, Alfredo

, p. 9236 - 9239 (2008)

(Chemical Equation Presented) Diels or no Diels? A bifunctional organic catalyst based on the thiourea motif is able to coordinate both diene and dienophile in an unprecedented asymmetric Diels-Alder reaction of 3-vinylindole derivatives, giving a rapid access to optically active tetra- and hexahydrocarbazoles with excellent results in terms of yields, diastereoselectivities, and enantioselectivities.

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