30369-21-2

Basic information

• Product Name: 4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-AMINE
• Synonyms: 4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-AMINE;4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-YLAMINE
• CAS NO: 30369-21-2
• Molecular Formula: C₁₅H₁₀Cl₂N₄
• Molecular Weight: 317.17
• Mol File: 30369-21-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 548.4°C at 760 mmHg
• Flash Point: 285.4°C
• Appearance: /
• Density: 1.404g/cm³
• Vapor Pressure: 4.46E-12mmHg at 25°C
• Refractive Index: 1.663
• CAS DataBase Reference: 4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-AMINE(30369-21-2)
• EPA Substance Registry System: 4,6-BIS(4-CHLOROPHENYL)-1,3,5-TRIAZIN-2-AMINE(30369-21-2)

Safety Data

• Hazardous Substances Data: 30369-21-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H10Cl2N4/c16-11-5-1-9(2-6-11)13-19-14(21-15(18)20-13)10-3-7-12(17)8-4-10/h1-8H,(H2,18,19,20,21)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 113-00-8 guanidine nitrate 
• 104-85-8 para-methylbenzonitrile 
• 14401-51-5 4-chlorobenzamidine hydrochloride 
• 30886-09-0 4,6-bis-(4-chloro-phenyl)-1H-[1,3,5]triazin-2-one 
• 30894-94-1 2-chloro-4,6-bis-(4-chloro-phenyl)-[1,3,5]triazine 
• 18916-77-3 p-toluimidoyl-guanidine 
• 64-17-5 ethanol 

Downstream Products

• 17584-14-4 4-amino-6-(4-chloro-phenyl)-1H-[1,3,5]triazin-2-one 

Relevant articles and documents

METHOD FOR PRODUCING 2-AMINO-1,3,5-TRIAZINE COMPOUND

PROBLEM TO BE SOLVED: To provide a method for producing 2-amino-4,6-di-substituted 1,3,5-triazine simply and under a mild condition. SOLUTION: Guanidine or a salt thereof is added to a mixture including a nitrile compound and a base and reacted therewith to produce 2-amino-4,6-di-substituted 1,3,5-triazine. Alternatively, a mixture (or a mixed liquid) including guanidine or a salt thereof and a solvent may be added to a mixture (or a mixed liquid) including a nitrile compound, a base and a solvent and reacted therewith. The base may be an alkali metal hydride, for example, sodium hydride. After completing the reaction, a step of depositing a deposit by adding a poor solvent to the reaction mixture and a step of separating the deposited deposit may be included. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT