Cas 79328-89-5,(1S,4S,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-aza-bicyclo[2.2.2]oct-7-ene-2,6-dicarboxylic acid 6-ethyl ester 2-(2,2,2-trichloro-ethyl) ester

79328-89-5

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Basic information

Product Name: (1S,4S,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-aza-bicyclo[2.2.2]oct-7-ene-2,6-dicarboxylic acid 6-ethyl ester 2-(2,2,2-trichloro-ethyl) ester
Synonyms:
CAS NO:79328-89-5
Molecular Formula:
Molecular Weight: 611.93
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: (1S,4S,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-aza-bicyclo[2.2.2]oct-7-ene-2,6-dicarboxylic acid 6-ethyl ester 2-(2,2,2-trichloro-ethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4S,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-aza-bicyclo[2.2.2]oct-7-ene-2,6-dicarboxylic acid 6-ethyl ester 2-(2,2,2-trichloro-ethyl) ester(79328-89-5)
EPA Substance Registry System: (1S,4S,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-aza-bicyclo[2.2.2]oct-7-ene-2,6-dicarboxylic acid 6-ethyl ester 2-(2,2,2-trichloro-ethyl) ester(79328-89-5)

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: 79328-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79328-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79328-89:
(7*7)+(6*9)+(5*3)+(4*2)+(3*8)+(2*8)+(1*9)=175
175 % 10 = 5
So 79328-89-5 is a valid CAS Registry Number.

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79328-89-5Relevant academic research and scientific papers

Diels-Alder Adducts of 1-Benzenesulfonylindole-2-acrylates and 1-(Alkoxycarbonyl)-1,2-dihydropyridines. Intermediates for Synthesis of Iboga Alkaloid Analogues

Sundberg, Richard J.,Bloom, Jonathan D.

, p. 4836 - 4842 (2007/10/02)

Diels-Alder reactions between methyl 1-benzenesulfonylindole-2-acrylate and several 1-(alkoxycarbonyl)-1,2-dihydropyridines give protected methyl 7-(2-indolyl)-2-azabicyclooctene-7-carboxylates which serve as intermediates for the synthesis of analogues of the iboga alkaloids.Methods for deprotection of both the carbamate nitrogen and indole nitrogen are reported.The 7-(2-indolyl)-2-azabicyclooctene-7-carboxylates show a tendency to undergo fragmentation of the C-1,C-7 bond of the 2-azabicyclooctene ring, probably by retro-Mannich reactions.Several 6-nor-20-deethyl analogues of catharanthine have been prepared from intermediates derived from the deprotected Diels-Alder adducts.

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