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2-phenoxy-4H-pyrido[1,2-a][1,3,5]triazin-4-one is a complex organic chemical compound with the molecular formula C12H7N3O2. It is a derivative of pyrido[1,2-a][1,3,5]triazine, a heterocyclic compound with a pyridine ring fused to a 1,3,5-triazine ring. The compound features a phenoxy group attached to the 2-position of the pyrido[1,2-a][1,3,5]triazine core, which contributes to its unique chemical properties. 2-phenoxy-4H-pyrido[1,2-a][1,3,5]triazin-4-one is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical products due to its specific structure and reactivity. However, further research and characterization are needed to fully understand its properties and potential uses.

5223-65-4

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5223-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5223-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5223-65:
(6*5)+(5*2)+(4*2)+(3*3)+(2*6)+(1*5)=74
74 % 10 = 4
So 5223-65-4 is a valid CAS Registry Number.

5223-65-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenoxypyrido[1,2-a][1,3,5]triazin-4-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:5223-65-4 SDS

5223-65-4Downstream Products

5223-65-4Relevant academic research and scientific papers

Metal-Free Domino One-Pot Decarboxylative Cyclization of Cinnamic Acid Esters: Synthesis of Functionalized Indanes

Gopi Krishna Reddy, Alavala,Satyanarayana, Gedu

, p. 12212 - 12222 (2016/12/23)

Trifluoroacetic acid promoted unprecedented domino reaction for the synthesis of diverse indanes starting from simple cinnamic acid esters is described. Their formation can be explained via acid triggered decarboxylation of cinnamic acid esters and subsequent inter/intramolecular cyclization. Overall process involves in the intramolecular cleavage of two σ-bonds (C-O and C-C) and inter/intramolecular construction of two/one C-C σ-bond(s). Significantly, this protocol was successful without the aid of any metal salts.

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