Cas 110699-01-9,2-(4-Methoxy-phenyl)-4-phenyl-4-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4H-oxazol-5-one

110699-01-9

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Basic information

Product Name: 2-(4-Methoxy-phenyl)-4-phenyl-4-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4H-oxazol-5-one
Synonyms:
CAS NO:110699-01-9
Molecular Formula:
Molecular Weight: 492.457
EINECS: N/A
Product Categories: N/A
Mol File: 110699-01-9.mol
Article Data: 1

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-(4-Methoxy-phenyl)-4-phenyl-4-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4H-oxazol-5-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Methoxy-phenyl)-4-phenyl-4-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4H-oxazol-5-one(110699-01-9)
EPA Substance Registry System: 2-(4-Methoxy-phenyl)-4-phenyl-4-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4H-oxazol-5-one(110699-01-9)

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: 110699-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110699-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110699-01:
(8*1)+(7*1)+(6*0)+(5*6)+(4*9)+(3*9)+(2*0)+(1*1)=109
109 % 10 = 9
So 110699-01-9 is a valid CAS Registry Number.

110699-01-9Upstream product

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110699-01-9Relevant articles and documents

υ-Triazolines, XXVIII. - Reactions of 1-Aryl-4,5-dihydro-4-methylene-5-morpholino-υ-triazoles with 2,4-Diaryl-5(4h)-oxazolones

Almirante, Nicoletta,Arlandini, Emanuele,Erba, Emanuela,Pocar, Donato,Trimarco, Pasqualina

, p. 1073 - 1078 (2007/10/02)

The 5(4H)-oxazolones 1a-d with an electron-rich aryl substituent on C-2 react with 4,5-dihydro-υ-triazoles 2a-c to afford the 4--5(4H)-oxazolones 3a-i as main reaction products and 2,5-diaryl-3-pyrrolecarbaldehydes 4a-d and glycine di

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