Cas 124016-55-3,(+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate

124016-55-3

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Basic information

Product Name: (+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate
Synonyms: (+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate
CAS NO:124016-55-3
Molecular Formula:
Molecular Weight: 418.449
EINECS: N/A
Product Categories: N/A
Mol File: 124016-55-3.mol
Article Data: 2

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: (+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate(124016-55-3)
EPA Substance Registry System: (+)-5-benzyl-11b-methyl (5S,11bR)-3-oxo-2,3,6,11-tetrahydro-1H-indolizino[8,7b]indole-5,11b(5H)-dicarboxylate(124016-55-3)

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: 124016-55-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124016-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,1 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124016-55:
(8*1)+(7*2)+(6*4)+(5*0)+(4*1)+(3*6)+(2*5)+(1*5)=83
83 % 10 = 3
So 124016-55-3 is a valid CAS Registry Number.

124016-55-3Upstream product

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124016-55-3Relevant articles and documents

Elaboration of vinblastine hybrids using a reactive in situ generated N-carboxyanhydride

Rannoux, Claire,Roussi, Fanny,Martin, Marie-Therese,Gueritte, Franoise

, p. 4873 - 4881 (2011/08/06)

Hybrids of vinblastine and phomopsin, designed by a molecular modelling study, were elaborated in order to target tubulin. The key step of the synthesis (fragmentation and insertion of vindoline) was mediated by an internal N-carboxyanhydride (or O-acylca

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