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2-(methylsulfanyl)-4,6-diphenyl-1,3,5-triazine is an organic compound with the molecular formula C15H13N3S. It is a derivative of the 1,3,5-triazine ring system, which is a heterocyclic aromatic compound consisting of three nitrogen atoms and three carbon atoms. In this specific compound, two of the carbon atoms in the triazine ring are substituted with phenyl groups (C6H5), and the third carbon atom is substituted with a methylsulfanyl group (CH3S). 2-(methylsulfanyl)-4,6-diphenyl-1,3,5-triazine is known for its potential applications in various chemical and pharmaceutical industries, as well as its use as an intermediate in the synthesis of other organic compounds. Due to its unique structure and properties, it has been the subject of research in the field of organic chemistry, with potential applications in the development of new drugs, dyes, and other specialty chemicals.

735-69-3

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735-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 735-69-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 735-69:
(5*7)+(4*3)+(3*5)+(2*6)+(1*9)=83
83 % 10 = 3
So 735-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H13N3S/c1-20-16-18-14(12-8-4-2-5-9-12)17-15(19-16)13-10-6-3-7-11-13/h2-11H,1H3

735-69-3Downstream Products

735-69-3Relevant academic research and scientific papers

Reactions of 2-Aryl(Alkyl)-4,6-bis(alkylthio)-1,3,5-oxadiazinium Salts with Nucleopiles

Herrmann, Dieter,Lohre, Wolfgang

, p. 1874 - 1881 (2007/10/02)

2-Aryl(Alkyl)-4,6-bis(alkylthio)-1,3,5-oxadiazinium salts 2 react with ammonia and amidines to give the derivatives 6,7, and 8 of 1,3,5-triazine.Reactions of 2 with hydrazine or hydrogen sulfide yield S-methyl N-(5-aryl-4H-1,2,4-triazol-3-yl)thiocarbamidates 5 or S-methyl N-(5-aryl-3H-1,2,4-dithiazol-3-ylidene)thiocarbamidates 9, respectively.

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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