Cas 126403-46-1,2-Cyano-4-(4-methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-allyl]-pent-4-enoic acid ethyl ester

126403-46-1

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Basic information

Product Name: 2-Cyano-4-(4-methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-allyl]-pent-4-enoic acid ethyl ester
Synonyms:
CAS NO:126403-46-1
Molecular Formula:
Molecular Weight: 405.494
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: 2-Cyano-4-(4-methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-allyl]-pent-4-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Cyano-4-(4-methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-allyl]-pent-4-enoic acid ethyl ester(126403-46-1)
EPA Substance Registry System: 2-Cyano-4-(4-methoxy-phenyl)-2-[2-(4-methoxy-phenyl)-allyl]-pent-4-enoic acid ethyl ester(126403-46-1)

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: 126403-46-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126403-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126403-46:
(8*1)+(7*2)+(6*6)+(5*4)+(4*0)+(3*3)+(2*4)+(1*6)=101
101 % 10 = 1
So 126403-46-1 is a valid CAS Registry Number.

126403-46-1Upstream product

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126403-46-1Relevant academic research and scientific papers

THE REACTION OF QUATERNARY AMMONIUM SALTS DERIVED FROM 2-ARYL-3-(N,N-DIMETHYLAMINO)-1-PROPENES WITH SOME ENOLATE ANIONS

Gupton, John T.,Krolikowski, Dale,Rusler, Mark

, p. 2415 - 2422 (2007/10/02)

A variety of quaternary ammonium salts derived from 2-aryl-3-(N,N-dimethylamino)-1-propenes have been reacted with enolate anions derived from several activated methylene compounds.The reactions represent clean and efficient methodology for the elaboration of the 2-aryl-1-propene system.

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