Cas 122409-75-0,2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one

122409-75-0

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Basic information

Product Name: 2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one
Synonyms:
CAS NO:122409-75-0
Molecular Formula:
Molecular Weight: 458.904
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-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one(122409-75-0)
EPA Substance Registry System: 2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one(122409-75-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 122409-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122409-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122409-75:
(8*1)+(7*2)+(6*2)+(5*4)+(4*0)+(3*9)+(2*7)+(1*5)=100
100 % 10 = 0
So 122409-75-0 is a valid CAS Registry Number.

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122409-75-0Downstream Products

122409-75-0Relevant academic research and scientific papers

Reaction of 5-Amino-4,5-dihydro-4-methylene-1,2,3-triazoles with 2,4-Diaryl-5(4H)-oxazolon-4-yl Radicals

Arlandini, Emanuele,Clerici, Francesca,Erba, Emanuela,Rossi, Luisa Maria

, p. 217 - 220 (2007/10/02)

When bioxazolones 2 are treated at high temperature with 5-amino-4,5-dihydrotriazoles 3, the corresponding triazolylmethyl-5(4H)-oxazolones 4 and 5 are produced by dissociation of 2 into oxazolonyl radicals and reaction of these with 3, followed by transf

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