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4,6-diphenoxy-N-phenyl-1,3,5-triazin-2-amine is a complex organic compound with the molecular formula C19H14N4O2. It is characterized by a triazine ring system, which is a six-membered aromatic ring containing three nitrogen atoms. The compound features two phenoxy groups attached at the 4 and 6 positions of the triazine ring, and a phenyl group is connected to the nitrogen atom at the 2 position. This chemical structure endows the compound with unique electronic and steric properties, which can be relevant in various chemical and pharmaceutical applications. The compound's specific reactivity, solubility, and potential uses in the synthesis of other compounds or as a building block in material science are areas of interest for researchers in the field.

1973-08-6

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1973-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1973-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1973-08:
(6*1)+(5*9)+(4*7)+(3*3)+(2*0)+(1*8)=96
96 % 10 = 6
So 1973-08-6 is a valid CAS Registry Number.

1973-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-diphenoxy-N-phenyl-1,3,5-triazin-2-amine

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:1973-08-6 SDS

1973-08-6Downstream Products

1973-08-6Relevant academic research and scientific papers

One-pot synthesis of triazines as potential agents affecting cell differentiation

Linder, Thomas,Schnürch, Michael,Mihovilovic, Marko D.

, p. 1257 - 1284 (2018)

Abstract: This paper outlines the synthesis of a number of structural analogs of 3-[(4,6-diphenoxy-1,3,5-triazin-2-yl)amino]benzoic acid which represent compounds with potential cardiogenetic activity. A one-pot protocol was developed for swift functionalization of the 1,3,5-triazine core without the need of isolating intermediates. The developed route starts from readily available 2,4,6-trichloro-1,3,5-triazine, displacing the chlorine atoms sequentially by aryloxy, arylamino, or arylthio moieties to enable access to molecules with three different substituents of this type in good yields. To facilitate purification, tert-butyl, methyl, and ethyl ester derivatives of the target compounds were initially synthesized. The tert-butyl esters could be readily hydrolyzed to the desired compounds, while reduction of the methyl and ethyl esters gave the corresponding benzylic alcohols in high yields, thereby expanding the substrate scope for future relevant cell assays. Graphical abstract: [Figure not available: see fulltext.].

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