Cas 583887-02-9,[1-(N-benzyl)-5-benzyloxy-pyridone-4-yl-2]-methyl(N-benzhydrylamino)phosphonic acid

583887-02-9

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Basic information

Product Name: [1-(N-benzyl)-5-benzyloxy-pyridone-4-yl-2]-methyl(N-benzhydrylamino)phosphonic acid
Synonyms:
CAS NO:583887-02-9
Molecular Formula:
Molecular Weight: 566.593
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: [1-(N-benzyl)-5-benzyloxy-pyridone-4-yl-2]-methyl(N-benzhydrylamino)phosphonic acid(CAS DataBase Reference)
NIST Chemistry Reference: [1-(N-benzyl)-5-benzyloxy-pyridone-4-yl-2]-methyl(N-benzhydrylamino)phosphonic acid(583887-02-9)
EPA Substance Registry System: [1-(N-benzyl)-5-benzyloxy-pyridone-4-yl-2]-methyl(N-benzhydrylamino)phosphonic acid(583887-02-9)

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: 583887-02-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 583887-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,3,8,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 583887-02:
(8*5)+(7*8)+(6*3)+(5*8)+(4*8)+(3*7)+(2*0)+(1*2)=209
209 % 10 = 9
So 583887-02-9 is a valid CAS Registry Number.

583887-02-9Upstream product

91-00-9 Benzhydrylamine

583887-02-9Downstream Products

112334-26-6 N-[[1,4-dihydro-4-oxo-5-(phenylmethoxy)-1-(phenylmethyl)-2-pyridinyl]methyl]amine

583887-02-9Relevant academic research and scientific papers

Synthesis and cleavage of pyridone-4 aminophosphonic acids

Boduszek, Bogdan,Korenova, Anna,Uher, Michal,Vegh, Daniel

, p. 1047 - 1053 (2003)

Some new pyridone aminophosphonic acids were synthesized from pyridone aldimines and tris(trimethylsilyl)phosphite. It was found that the obtained aminophosphonic acids 2 were cleaved in mineral acid solutions to form the corresponding amines 3 and phosphoric acid. Preliminary kinetic measurements were performed.

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