Cas 106367-83-3,(3aR,10bR,11R,12bR)-3a-Ethyl-6-(4-methoxy-benzenesulfonyl)-11-phenylsulfanyl-2,3,3a,4,6,12b-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-12-thione

106367-83-3

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Basic information

Product Name: (3aR,10bR,11R,12bR)-3a-Ethyl-6-(4-methoxy-benzenesulfonyl)-11-phenylsulfanyl-2,3,3a,4,6,12b-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-12-thione
Synonyms:
CAS NO:106367-83-3
Molecular Formula:
Molecular Weight: 588.816
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)-3a-Ethyl-6-(4-methoxy-benzenesulfonyl)-11-phenylsulfanyl-2,3,3a,4,6,12b-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-12-thione(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,10bR,11R,12bR)-3a-Ethyl-6-(4-methoxy-benzenesulfonyl)-11-phenylsulfanyl-2,3,3a,4,6,12b-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-12-thione(106367-83-3)
EPA Substance Registry System: (3aR,10bR,11R,12bR)-3a-Ethyl-6-(4-methoxy-benzenesulfonyl)-11-phenylsulfanyl-2,3,3a,4,6,12b-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-12-thione(106367-83-3)

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: 106367-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106367-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,6 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106367-83:
(8*1)+(7*0)+(6*6)+(5*3)+(4*6)+(3*7)+(2*8)+(1*3)=123
123 % 10 = 3
So 106367-83-3 is a valid CAS Registry Number.

106367-83-3Upstream product

85924-17-0 (+/-)-2,3-didehydro-1-<(p-methoxyphenyl)sulfonyl>-11β-phenylthio-aspidospermidin-10-one

106367-83-3Downstream Products

106367-83-3Relevant academic research and scientific papers

METHODS FOR INDOLE ALKALOID SYNTHESIS: REACTIONS OF N-ARYLSULFONYLENAMINES WITH ELECTROPHILES. AN EXPEDITIOUS SYNTHESIS OF (+/-)-EBURNAMONINE.

Magnus, Philip,Pappalardo, Paul,Southwell, Ian

, p. 3215 - 3222 (2007/10/02)

Treatment of 4 with MCPBA gave 9.The pentacyclic amide 3 on exposure to cyanogen chloride gave the cis-chloro-hydrin 20, and the geminal dichloride 21.When 21 was treated with HCl/MeOH it rapidly rearranged to eburnamonine lactam 22.

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