Cas 879885-75-3,5-(α-phenylethylaminodiethoxyphosphorylmethyl)-25,27-dipropoxycalix[4]arene

879885-75-3

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Basic information

Product Name: 5-(α-phenylethylaminodiethoxyphosphorylmethyl)-25,27-dipropoxycalix[4]arene
Synonyms:
CAS NO:879885-75-3
Molecular Formula:
Molecular Weight: 777.938
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: 5-(α-phenylethylaminodiethoxyphosphorylmethyl)-25,27-dipropoxycalix[4]arene(CAS DataBase Reference)
NIST Chemistry Reference: 5-(α-phenylethylaminodiethoxyphosphorylmethyl)-25,27-dipropoxycalix[4]arene(879885-75-3)
EPA Substance Registry System: 5-(α-phenylethylaminodiethoxyphosphorylmethyl)-25,27-dipropoxycalix[4]arene(879885-75-3)

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: 879885-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 879885-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,8,8 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 879885-75:
(8*8)+(7*7)+(6*9)+(5*8)+(4*8)+(3*5)+(2*7)+(1*5)=273
273 % 10 = 3
So 879885-75-3 is a valid CAS Registry Number.

879885-75-3Upstream product

762-04-9 phosphonic acid diethyl ester

879885-75-3Downstream Products

879885-75-3Relevant academic research and scientific papers

Calix[4]arene α-aminophosphonic acids: Asymmetric synthesis and enantioselective inhibition of an alkaline phosphatase

Cherenok, Sergiy,Vovk, Andriy,Muravyova, Iryna,Shivanyuk, Alexander,Kukhar, Valery,Lipkowski, Janusz,Kalchenko, Vitaly

, p. 549 - 552 (2006)

Chiral calix[4]arene α-aminophosphonic acids were obtained through diastereoselective Pudovik-type addition of sodium ethyl phosphites to the chiral calixarene imines, removal of chiral auxiliary groups, and mild dealkylation of phosphonate fragments. The

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