Cas 1453187-84-2,ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate

1453187-84-2

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Basic information

Product Name: ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate
Synonyms: ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate
CAS NO:1453187-84-2
Molecular Formula:
Molecular Weight: 425.484
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: ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate(1453187-84-2)
EPA Substance Registry System: ethyl (E)-3-{(Z)-1-[(4-methoxyphenyl)imino]-3-phenyl-1H-isochromen-4-yl}acrylate(1453187-84-2)

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: 1453187-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1453187-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,1,8 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1453187-84:
(9*1)+(8*4)+(7*5)+(6*3)+(5*1)+(4*8)+(3*7)+(2*8)+(1*4)=172
172 % 10 = 2
So 1453187-84-2 is a valid CAS Registry Number.

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1453187-84-2Relevant academic research and scientific papers

A practical protocol for three-component, one-pot, stepwise sonogashira-heterocyclization-heck couplings

Madich, Youssef,Denis, J.Gabriel,Ortega, Aitor,Martinez, Claudio,Matrane, Abdellatif,Belachemi, Larbi,De Lera, Angel R.,Alvarez, Rosana,Aurrecoechea, Jose M.

, p. 2009 - 2017 (2013/07/26)

A three-component, one-pot, stepwise Sonogashira-heterocyclization-Heck- coupling process was developed starting from either haloarenecarboxamides, halophenols or haloanilines, terminal alkynes and electron-deficient alkenes. Cyclic imidate-, benzofuran-,

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