Cas 1218989-83-3,butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate

1218989-83-3

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Basic information

Product Name: butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate
Synonyms: butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate
CAS NO:1218989-83-3
Molecular Formula:
Molecular Weight: 570.666
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: butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate(CAS DataBase Reference)
NIST Chemistry Reference: butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate(1218989-83-3)
EPA Substance Registry System: butyl (E)-3-(3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-1-(4-methylbenzene-sulfonyl)-1H-indol-2-yl)acrylate(1218989-83-3)

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: 1218989-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1218989-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,9,8 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1218989-83:
(9*1)+(8*2)+(7*1)+(6*8)+(5*9)+(4*8)+(3*9)+(2*8)+(1*3)=203
203 % 10 = 3
So 1218989-83-3 is a valid CAS Registry Number.

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1218989-83-3Relevant academic research and scientific papers

Gold(I)-catalyzed tandem cyclization approach to tetracyclic indolines

Liu, Yongxiang,Xu, Wenqing,Wang, Xiang

supporting information; experimental part, p. 1448 - 1451 (2010/06/20)

Chemical equation presented Two highly stereoselective cationic gold(I)-catalyzed tandem cyclization reactions of alkynylindoles are described. These reactions demonstrated a novel and general strategy to rapidly construct highly functionalized polycyclic indolines. This approach was successfully employed for a formal synthesis of the akuammiline alkaloid minfiensine.

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