Cas 139259-15-7,1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4-<p-nitrophenyl> quinolizine

139259-15-7

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Basic information

Product Name: 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine
Synonyms: 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine
CAS NO:139259-15-7
Molecular Formula:
Molecular Weight: 419.437
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: 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine(CAS DataBase Reference)
NIST Chemistry Reference: 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine(139259-15-7)
EPA Substance Registry System: 1,2,3,4,6,7,12,12b-octahydro-2-oxoindolo<2,3-a>-(4R,6S,12bR)-6-carboxymethyl-4- quinolizine(139259-15-7)

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: 139259-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139259-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139259-15:
(8*1)+(7*3)+(6*9)+(5*2)+(4*5)+(3*9)+(2*1)+(1*5)=147
147 % 10 = 7
So 139259-15-7 is a valid CAS Registry Number.

139259-15-7Upstream product

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139259-15-7Relevant academic research and scientific papers

Asymmetric Synthesis of Indoloquinolizidin-2-ones Congeners to Yohimbine-Type Alkaloids

Waldmann, Herbert,Braun, Matthias,Weymann, Markus,Gewehr, Markus

, p. 397 - 416 (2007/10/02)

Schiff bases derived from tryptophan methyl ester and tryptamine react with Danishefkys diene in the presence of ZnCl2 to give enaminones which are subsequently transformed into indoloquinolizidin-2-ones by acid-catalyzed cyclization.These tetracyc

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