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1,3,5-Triazin-2-amine, 4-ethoxy-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61903-35-3

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61903-35-3 Usage

General Description

1,3,5-Triazin-2-amine, 4-ethoxy-6-phenyl-, also known as ethopabate, is a chemical compound that belongs to the class of triazine compounds. It is commonly used as a coccidiostat, which means it is a substance that can suppress the growth of coccidian parasites in animals. Ethopabate is primarily used in the agriculture industry, specifically in the poultry sector, to prevent and treat coccidiosis in chickens. It works by inhibiting the development and reproduction of coccidian parasites, ultimately protecting the health and productivity of the birds. Additionally, ethopabate has been found to have low toxicity and minimal adverse effects on non-target organisms, making it a valuable and effective tool for controlling coccidiosis in poultry farming.

Check Digit Verification of cas no

The CAS Registry Mumber 61903-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,0 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61903-35:
(7*6)+(6*1)+(5*9)+(4*0)+(3*3)+(2*3)+(1*5)=113
113 % 10 = 3
So 61903-35-3 is a valid CAS Registry Number.

61903-35-3Relevant academic research and scientific papers

Reactions with N-Acylimino-dithiocarbonic-acid-diesters

Augustin, M.,Richter, M.,Salas, S.

, p. 55 - 68 (2007/10/02)

Reactions of N-acylimino-dithiocarbonic-acid-S,S-diesters 1 with nucleophilic compounds present new possibilities to synthesize heterocycles.With amines 1a reacts by mono- and disubstitution, respectively, of methylthio-groups to isothioureas 2 and guanidines 3, with 1,2-binucleophilic arenes to benzoheterocycles 4, with aliphatic diamines to imidazolines 5, pyrimidines 6, diazepines 7 and the hexamethylene-diamine-derivatives 8. 1a reacts also with hydrazines to 1,2,4-triazoles 9 and with hydrazides to the thiosemicarbazones 10 or 1,3,4-oxadiazoles 11.Heterocyclisations of 1 with guanidines, thiourea, salts of thiourea and amidines give the 1,3,5-triazines 12, 14, 15 and 16.N-benzoyl-dithiocarbonic-acid-methylester -amid reacts with CH-acidic compounds to thiazoles 17.The structures of the final products are determined by i.r.-, 1H-n.m.r.-, u.v.- and mass-spectras.

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