3114-52-1

Basic information

• Product Name: 2-(P-CHLOROPHENYL)-4,6-DIPHENYL-S-TRIAZINE
• Synonyms: 2-(P-CHLOROPHENYL)-4,6-DIPHENYL-S-TRIAZINE;2-(4-chlorophenyl)-4,6-diphenyl-1,3,5-Triazine
• CAS NO: 3114-52-1
• Molecular Formula: C₂₁H₁₄ClN₃
• Molecular Weight: 343.81
• Mol File: 3114-52-1.mol
• Article Data: 31

Chemical Properties

• Boiling Point: 561°Cat760mmHg
• Flash Point: 322.5°C
• Appearance: /
• Density: 1.241g/cm³
• Vapor Pressure: 4.87E-12mmHg at 25°C
• Refractive Index: 1.635
• PKA: 0.45±0.10(Predicted)
• CAS DataBase Reference: 2-(P-CHLOROPHENYL)-4,6-DIPHENYL-S-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(P-CHLOROPHENYL)-4,6-DIPHENYL-S-TRIAZINE(3114-52-1)
• EPA Substance Registry System: 2-(P-CHLOROPHENYL)-4,6-DIPHENYL-S-TRIAZINE(3114-52-1)

Safety Data

• Hazardous Substances Data: 3114-52-1(Hazardous Substances Data)

Usage

General Description

2-(p-chlorophenyl)-4,6-diphenyl-s-triazine, also known as Monuron, is a chemical compound used as a herbicide. It is a white crystalline solid with a faint odor, and is highly soluble in organic solvents. Monuron works by inhibiting photosynthesis in plants, preventing them from producing the energy they need to grow. It is commonly used in agriculture to control weeds in crops such as cotton and soybeans, as well as in non-agricultural settings like golf courses and industrial sites. However, due to its potential to harm aquatic organisms and its persistence in the environment, the use of Monuron has become increasingly restricted in some countries.

InChI:InChI=1/C21H14ClN3/c22-18-13-11-17(12-14-18)21-24-19(15-7-3-1-4-8-15)23-20(25-21)16-9-5-2-6-10-16/h1-14H

Upstream product

• 5496-32-2 2-(4-chlorophenyl)-4,5-diphenyl-1H-imidazole 
• 98-80-6 phenylboronic acid 
• 3842-55-5 2-chloro-4,6-diphenyl-1,3,5-triazine 
• 1679-18-1 4-Chlorophenylboronic acid 
• 1670-14-0 benzamidine monohydrochloride 
• 104-88-1 4-chlorobenzaldehyde 
• 873-76-7 para-Chlorobenzyl alcohol 
• 108-86-1 bromobenzene 
• 620-40-6 tribenzylamine 
• 14401-51-5 4-chlorobenzamidine hydrochloride 
• 106-43-4 para-chlorotoluene 
• 104-11-0 N-methyl-4-chlorobenzylamine 
• 99-91-2 para-chloroacetophenone 
• 1878-66-6 4-chlorophenylacetic Acid 

Downstream Products

• 1345202-07-4 C₅₁H₃₃N₅ 
• 1219956-23-6 2,4-diphenyl-6-(4-(4_,4_',5,5'-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine 

Relevant articles and documents

Organic compound and organic electroluminescent device containing same

The invention relates to an organic compound, which is characterized by having a structure as shown in (1), wherein L1 and L2 are respectively and independently selected from a single bond, a substituted or unsubstituted C6-C30 arylene group or a substituted or unsubstituted C3-C30 heteroarylene group; Arl and Ar2 are respectively and independently selected from a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; R is halogen, a cyano group, an alkyl group, a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; and n represents an integer of 0-3.

Organic compound, electronic element and electronic device

The invention provides an organic compound, and belongs to the technical field of organic materials. According to the compound disclosed by the invention, an electron-deficient nitrogen-containing heteroaryl group and a cyano group are connected to a stru

An alternatively metal-free synthesis of 1,3,5-triazines or 1,2,4-thiadiazoles from benzyl chlorides and benzylamines mediated by elemental sulfur

An elemental sulfur mediated reaction of benzyl chlorides with benzylamines is developed, which allows the practical synthesis of valuable 1,3,5-triazines. This protocol that is metal free, ligand free, and uses inexpensive elemental sulfur as oxidant or raw material displays mild reaction conditions, a broad substrate scope and moderate to good yields. Moreover, the modified sulfur-mediated reaction system can also be used to synthesize 1,2,4-thiadiazoles, by simply switching the stoichiometry of sulfur powder from 0.75 equivalents to 5 equivalents.