69466-88-2

Basic information

• Product Name: 5,6-Bis(p-chlorophenyl)-3-methylthio-1,2,4-triazine
• Synonyms: 5,6-Bis(p-chlorophenyl)-3-methylthio-1,2,4-triazine
• CAS NO: 69466-88-2
• Molecular Formula: C₁₆H₁₁Cl₂N₃S
• Molecular Weight: 348.2496
• Mol File: 69466-88-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 505.7°Cat760mmHg
• Flash Point: 259.6°C
• Appearance: /
• Density: 1.44g/cm³
• Vapor Pressure: 7.51E-10mmHg at 25°C
• Refractive Index: 1.69
• CAS DataBase Reference: 5,6-Bis(p-chlorophenyl)-3-methylthio-1,2,4-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-Bis(p-chlorophenyl)-3-methylthio-1,2,4-triazine(69466-88-2)
• EPA Substance Registry System: 5,6-Bis(p-chlorophenyl)-3-methylthio-1,2,4-triazine(69466-88-2)

Safety Data

• Hazardous Substances Data: 69466-88-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H11Cl2N3S/c1-22-16-19-14(10-2-6-12(17)7-3-10)15(20-21-16)11-4-8-13(18)9-5-11/h2-9H,1H3

Upstream product

• 79-19-6 thiosemicarbazide 
• 3457-46-3 4,4'-dichlorobenzil 
• 74-88-4 methyl iodide 
• 35600-34-1 S-methyl isothiosemicarbazide hydroiodide 
• 44387-06-6 methyl hydrazinecarbimidothioate 

Downstream Products

• 69467-22-7 3-methoxy-5,6-bis(p-chlorophenyl)-1,2,4-triazine 
• 74930-12-4 5,6-Bis-(4-chloro-phenyl)-3-methylsulfanyl-2,5-dihydro-[1,2,4]triazine 
• 74930-21-5 (S)-5,6-Bis-(4-chloro-phenyl)-3-methoxy-2-methyl-2,5-dihydro-[1,2,4]triazine 
• 74930-20-4 5,6-Bis-(4-chloro-phenyl)-2-methyl-3-methylsulfanyl-2,5-dihydro-[1,2,4]triazine 
• 74930-13-5 5,6-Bis-(4-chloro-phenyl)-3-methoxy-2,5-dihydro-[1,2,4]triazine 

Relevant articles and documents

CO2-assisted synthesis of non-symmetric α-diketones directly from aldehydes: Via C-C bond formation

CO2-assisted various symmetric and non-symmetric α-diketones have been synthesized directly from the corresponding aldehydes using transition metal-free catalysts. This method can even be applied to synthesize pharmaceuticals directly from aldehydes. The crucial role of CO2 has been investigated in detail and the mechanism is proposed on the basis of experiments and DFT calculations.

In vitro antitumor activity evaluation of some 1,2,4-triazine derivatives bearing piperazine amide moiety against breast cancer cells

A series of 1,2,4-triazine derivatives bearing piperazine amide moiety has been synthesized and investigated for their potential anticancer activities. 1-[4-(5,6-Bis(4-subtituted phenyl)-1,2,4-triazin-3-yl)piperazin-1-yl]-2-[4-(3-substituted phenyl)pipera

Room-temperature ionic liquid-DMSO promoted and improved one-pot synthesis of 5,6-diaryl-1,2,4-triazines

An improved and rapid one-pot synthesis of 5,6-diarylsubstituted-1,2,4- triazines in a mixture of room-temperature ionic liquid 1,3-dibutylimidazolium bromide [Bbim]+Br- and dimethylsulfoxide (DMSO) is described without the need for