Cas 85924-28-3,(3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one

85924-28-3

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Product Name: (3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one
Synonyms: (3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one
CAS NO:85924-28-3
Molecular Formula:
Molecular Weight: 560.695
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: (3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one(85924-28-3)
EPA Substance Registry System: (3aR,10bR,11R,12bR)-11-Benzenesulfinyl-6-(4-methoxy-benzenesulfonyl)-2,3,3a,4,6,11,12,12b-octahydro-6,12a-diaza-indeno[7,1-cd]fluoren-1-one(85924-28-3)

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: 85924-28-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85924-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,2 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85924-28:
(7*8)+(6*5)+(5*9)+(4*2)+(3*4)+(2*2)+(1*8)=163
163 % 10 = 3
So 85924-28-3 is a valid CAS Registry Number.

85924-28-3Upstream product

85924-28-3Downstream Products

85924-27-2 (+/-)-2,3,10,11-tetrahydro-1-<(p-methoxyphenyl)sulfonyl>-20,21-dinoraspidospermidin-8-one

85924-28-3Relevant academic research and scientific papers

Pentacyclic Systems for Indole Alkaloids. Formation of the C11-C12 Bond. Two Synthesis of (+/-)-Aspidospermine

Gallagher, Timothy,Magnus, Philip,Huufman, John C.

, p. 4750 - 4757 (2007/10/02)

The tetracyclic amide 10 was converted through an intramolecular Pummerer reaction into the petacyclic amide11, having the basic framework of the Aspidosperma alkaloids.Application of this methodology to the synthesis of (+/-)-aspidosper

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