3114-54-3

Basic information

• Product Name: 2,4,6-TRIS(P-CHLOROPHENYL)-S-TRIAZINE
• Synonyms: 2,4,6-TRIS(P-CHLOROPHENYL)-S-TRIAZINE;2,4,6-tris(4-chlorophenyl)-1,3,5-triazine
• CAS NO: 3114-54-3
• Molecular Formula: C₂₁H₁₂Cl₃N₃
• Molecular Weight: 412.7
• Mol File: 3114-54-3.mol
• Article Data: 10

Chemical Properties

• Melting Point: 327-328 °C
• Boiling Point: 597.1°Cat760mmHg
• Flash Point: 342.4°C
• Appearance: /
• Density: 1.371g/cm³
• Vapor Pressure: 1.38E-13mmHg at 25°C
• Refractive Index: 1.644
• PKA: -0.01±0.10(Predicted)
• CAS DataBase Reference: 2,4,6-TRIS(P-CHLOROPHENYL)-S-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-TRIS(P-CHLOROPHENYL)-S-TRIAZINE(3114-54-3)
• EPA Substance Registry System: 2,4,6-TRIS(P-CHLOROPHENYL)-S-TRIAZINE(3114-54-3)

Safety Data

• Hazardous Substances Data: 3114-54-3(Hazardous Substances Data)

Usage

General Description

2,4,6-Tris(p-chlorophenyl)-s-triazine is a chemical compound commonly used as an intermediate in the synthesis of various substances such as dyes, pigment, and pharmaceuticals. It is a member of the triazine class of compounds, which are characterized by a six-membered ring containing alternating carbon and nitrogen atoms. This specific compound is notable for its three p-chlorophenyl groups attached to the s-triazine ring, giving it unique properties and reactivity. It is primarily used as a precursor in the production of herbicides, notably atrazine, a widely used agricultural pesticide. 2,4,6-Tris(p-chlorophenyl)-s-triazine is considered to be a hazardous substance and should be handled with care due to its potential health and environmental risks.

InChI:InChI=1/C21H12Cl3N3/c22-16-7-1-13(2-8-16)19-25-20(14-3-9-17(23)10-4-14)27-21(26-19)15-5-11-18(24)12-6-15/h1-12H

Upstream product

• 105-56-6 ethyl 2-cyanoacetate 
• 827-72-5 4-chlorobenzimidic acid ethyl ester 
• 623-03-0 4-Cyanochlorobenzene 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 108-88-3 toluene 
• 104-88-1 4-chlorobenzaldehyde 
• 1498-66-4 N,N'-Bis<4-chlorobenzylidene>-4-chlorophenylmethanediamine 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 108-90-7 chlorobenzene 

Downstream Products

• 1498-38-0 2,4,5-tris(4-chlorophenyl)-1H-imidazole 

Relevant articles and documents

Preparation method of multipurpose compound s-triazine derivative

The invention provides a preparation method of a s-triazine derivative, which is characterized in that an aryl nitrile compound is used as a substrate, lithium bis (trifluoromethanesulfonimide) is used as a catalyst, and the s-triazine derivative is obtained through a cyclopolymerization reaction. Compared with the prior art, the method has the advantages that a catalytic system is simple and easy to obtain, too high or too low rigorous reaction temperature is not needed, the reaction condition is mild, the reaction time is short, the post-treatment is simple, and the obtained s-triazine derivative has very high yield and is suitable for large-scale production.

Pigment composition for a color filter and a color filter (by machine translation)

[Problem] excellent contrast color filter and color filter suitable for a pigment composition. The diketopyrrolopyrrole-based pigment [a], (I) a triazine compound represented by the formula containing a pigment composition for a color filter. [Drawing] no (by machine translation)

Addition of amines to nitriles catalyzed by ytterbium amides: An efficient one-step synthesis of monosubstituted N-arylamidines

A one-step synthesis of monosubstituted N-arylamidinates via addition of amines to nitriles catalyzed by ytterbium amides is reported. The reactions with various substrates give the products in good to excellent yields with 5 mol % ytterbium at 100 °C under solvent-free conditions.