Cas 228249-01-2,E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide

228249-01-2

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Basic information

Product Name: E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide
Synonyms: E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide
CAS NO:228249-01-2
Molecular Formula:
Molecular Weight: 404.403
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: E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide(CAS DataBase Reference)
NIST Chemistry Reference: E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide(228249-01-2)
EPA Substance Registry System: E-2-(diethylphosphonyl)-N-(p-methoxyphenyl)-3-(N-phenylamino)prop-2-enamide(228249-01-2)

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: 228249-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 228249-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,2,4 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 228249-01:
(8*2)+(7*2)+(6*8)+(5*2)+(4*4)+(3*9)+(2*0)+(1*1)=132
132 % 10 = 2
So 228249-01-2 is a valid CAS Registry Number.

228249-01-2Upstream product

228249-01-2Downstream Products

228249-10-3 diethyl 4-p-methoxyphenylaminoquinoline-3-phosphonate

228249-01-2Relevant academic research and scientific papers

A simple synthesis of 3-phosphonyl-4-aminoquinolines from β- enaminophosphonates

Palacios, Francisco,Ochoa De Retana, Ana M.,Oyarzabal, Julen

, p. 5947 - 5964 (2007/10/03)

An easy and efficient synthesis of 4-aminoquinolines substituted with a phosphorylated group or a phosphine oxide group in the 3-position is described. The key step is a regioselective addition of lithiated β-enamino phosphonates to isocyanates to give fu

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