Cas 85924-22-7,(4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one

85924-22-7

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Basic information

Product Name: (4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one
Synonyms: (4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one
CAS NO:85924-22-7
Molecular Formula:
Molecular Weight: 530.733
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: (4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one(85924-22-7)
EPA Substance Registry System: (4aR,11cS)-1-(2,2-Bis-methylsulfanyl-ethyl)-7-(4-methoxy-benzenesulfonyl)-4,4a,5,6,7,11c-hexahydro-1H,3H-pyrido[3,2-c]carbazol-2-one(85924-22-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 85924-22-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85924-22-7 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 85924-22:
(7*8)+(6*5)+(5*9)+(4*2)+(3*4)+(2*2)+(1*2)=157
157 % 10 = 7
So 85924-22-7 is a valid CAS Registry Number.

85924-22-7Upstream product

85924-22-7Downstream Products

85924-25-0 (+/-)-2,3-didehydro-1-<(p-methoxyphenyl)sulfonyl>-11β-(methylthio)-20,21-dinoraspidospermidin-8-one

85924-22-7Relevant 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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