Cas 135574-06-0,(Z)-2-(3-{2-[Benzyl-((E)-3-oxo-but-1-enyl)-amino]-ethyl}-1H-indol-2-yl)-but-2-enedioic acid dimethyl ester

135574-06-0

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Basic information

Product Name: (Z)-2-(3-{2-[Benzyl-((E)-3-oxo-but-1-enyl)-amino]-ethyl}-1H-indol-2-yl)-but-2-enedioic acid dimethyl ester
Synonyms:
CAS NO:135574-06-0
Molecular Formula:
Molecular Weight: 460.53
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: (Z)-2-(3-{2-[Benzyl-((E)-3-oxo-but-1-enyl)-amino]-ethyl}-1H-indol-2-yl)-but-2-enedioic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(3-{2-[Benzyl-((E)-3-oxo-but-1-enyl)-amino]-ethyl}-1H-indol-2-yl)-but-2-enedioic acid dimethyl ester(135574-06-0)
EPA Substance Registry System: (Z)-2-(3-{2-[Benzyl-((E)-3-oxo-but-1-enyl)-amino]-ethyl}-1H-indol-2-yl)-but-2-enedioic acid dimethyl ester(135574-06-0)

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: 135574-06-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135574-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,7 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135574-06:
(8*1)+(7*3)+(6*5)+(5*5)+(4*7)+(3*4)+(2*0)+(1*6)=130
130 % 10 = 0
So 135574-06-0 is a valid CAS Registry Number.

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135574-06-0Relevant academic research and scientific papers

19-hydroxytubotaiwine : Total synthesis. Assignment of absolute configuration to a natural isomer

Nkiliza, Jean,Vercauteren, Joseph,Leger, Jean-Michel

, p. 1787 - 1790 (1991)

A total synthesis of two isomers of racemic 19-hydroxytubotaiwine from tryptamine is described1. The absolute configuration of one of the two natural ones is defined by a NMR and X-ray study of intermediate.

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