4511-99-3

Basic information

• Product Name: 3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE
• Synonyms: 3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE;5,6-DIPHENYL-1,2,4-TRIAZIN-3-AMINE;3-amino-3,6-diphenyl-as-triazin;3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE 97%
• CAS NO: 4511-99-3
• Molecular Formula: C₁₅H₁₂N₄
• Molecular Weight: 248.28
• Mol File: 4511-99-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 177 °C
• Boiling Point: 463.6°Cat760mmHg
• Flash Point: 265.2°C
• Appearance: /
• Density: 1.229g/cm³
• Vapor Pressure: 8.94E-09mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE(4511-99-3)
• EPA Substance Registry System: 3-AMINO-5,6-DIPHENYL-1,2,4-TRIAZINE(4511-99-3)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 4511-99-3(Hazardous Substances Data)

Usage

General Description

3-Amino-5,6-diphenyl-1,2,4-triazine is a chemical compound with the formula C15H11N5. It falls under the category of triazines, organic compounds that consist of a six-membered ring that contains three carbon atoms and three nitrogen atoms. This chemical is not abundantly used or studied, so information on its properties, applications, and hazards is limited. However, similar compounds are often used in the manufacturing of dyes, pharmaceuticals, and other chemicals. Typically, triazines are synthetic and not found naturally in the environment, and some can be harmful or toxic. Specific safety and handling measures for 3-Amino-5,6-diphenyl-1,2,4-triazine would likely need to be determined experimentally.

InChI:InChI=1/C15H12N4/c16-15-17-13(11-7-3-1-4-8-11)14(18-19-15)12-9-5-2-6-10-12/h1-10H,(H2,16,17,19)

Upstream product

• 2582-30-1 aminoguanidine bicarbonate 
• 134-81-6 benzil 
• 83413-00-7 3-(methylsulfonyl)-5-phenyl-1,2,4-triazine 
• 942-60-9 5-phenyl-1,2,4-triazin-3-amine 
• 28735-27-5 3-methylthio-5-phenyl-1,2,4-triazine 
• 1321517-51-4 6-bromo-5-phenyl-1,2,4-triazin-3-amine 
• 98-80-6 phenylboronic acid 
• 272773-77-0 C₂₁H₂₅N₆O₃P 
• 88281-91-8 3-azido-5,6-diphenyl-1,2,4-triazine 
• 10308-82-4 aminoguanidine nitrate 
• 34177-11-2 3-chloro-5,6-diphenyl-1,2,4-triazine 

Downstream Products

• 108595-51-3 6-[1]naphthyl-2,3,7-triphenyl-imidazo[1,2-b][1,2,4]triazine 
• 4512-05-4 N-(5,6-diphenyl-[1,2,4]triazin-3-yl)-diacetamide 
• 10243-70-6 2,3,6-triphenyl-imidazo[1,2-b][1,2,4]triazine 
• 70111-81-8 2,3,6,7-tetraphenyl-imidazo[1,2-b][1,2,4]triazine 
• 20375-99-9 4-amino-N-(5,6-diphenyl-[1,2,4]triazin-3-yl)-benzenesulfonamide 
• 107613-72-9 6-Hydroxy-2,3-diphenyl-pyrimido[1,2-b][1,2,4]triazin-8-one 
• 107613-78-5 7-Benzyl-6-hydroxy-2,3-diphenyl-pyrimido[1,2-b][1,2,4]triazin-8-one 
• 107613-77-4 7-Ethyl-6-hydroxy-2,3-diphenyl-pyrimido[1,2-b][1,2,4]triazin-8-one 
• 107613-73-0 7-Butyl-6-hydroxy-2,3-diphenyl-pyrimido[1,2-b][1,2,4]triazin-8-one 
• 91028-81-8 2,3-Diphenyl-6-(4-bromophenyl)-7-bromoimidazo<1,2-b>-1,2,4-triazine 
• 70111-77-2 2,3,6-Triphenyl-7-bromoimidazo<1,2-b>-1,2,4-triazine 
• 115125-27-4 2-methyl-5,6-diphenyl-1,2,4-triazin-3(2H)-imine hydriodide 
• 21134-91-8 5,6-diphenyl-1,2,4-triazine 
• 34177-11-2 3-chloro-5,6-diphenyl-1,2,4-triazine 

Relevant articles and documents

Synthesis and reactions of 1,2,4-triazine azides with triphenylphosphine, trialkyl phosphites and dialkyl phosphonates

3-Azido-5,6-diphenyl-1,2,4-triazine (1) and 3-azidophenanthro[9,10-e]-1,2,4-triazine (2) are synthesized in high yield (-75%), 1 and 2 react with triphenylphosphine to afford phosphazenes 5 and 6 with a covalent structure. Reactions of 1 and 2 with trialkyl phosphites 3b,c produce phosphazenes 7a,b and 8a,b which have the phosphonium dipolar ion structure, 1 reacts with diethyl phosphonate (4a) to give the phosphoramidate 10a, dissociating to the corresponding amine 11 on reaction with dimethyl phosphonate. Possible reaction mechanisms are proposed for the formation of the new adducts.

Synthesis, spectroscopic (UV-vis and GIAO NMR), crystallographic and theoretical studies of triazine heterocyclic derivatives

Abstract This work presents the synthesis and characterization of triazine heterocyclic derivatives. The spectroscopic properties like nuclear magnetic resonance [NMR, (1H and 13C)] were recorded in CDCl3 solution and Ultr

1,2,4-TRIAZINE-4-AMINE DERIVATIVES

According to the invention there is provided a compound of formula A1 which may be useful in the treatment of a condition or disorder ameliorated by the inhibition of the A1- A2b or, particularly, the A2a receptor wherein the compound of formula A1 has the structure, wherein, A represents Cy1 or HetA; Cy1 represents a 5- to 14-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one, two or three rings, which Cy1 group is optionally substituted by one or more R4a substituents; HetA represents a 5- to 14-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one, two or three rings and which HetA group is optionally substituted by one or more R4b substituents; B represents a Cy2 or HetB; Cy2 represents a 3- to 10-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one or two rings, which Cy2 group is optionally substituted by one or more R4c substituents; HetB represents a 3- to 10-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one or two rings and which HetB group is optionally substituted by one or more R4d substituents.