28735-28-6

Basic information

• Product Name: 3-methoxy-5-phenyl-1,2,4-triazine
• Synonyms: 3-Methoxy-5-phenyl-1,2,4-triazine;5-26-03-00299 (Beilstein Handbook Reference)
• CAS NO: 28735-28-6
• Molecular Formula: C₁₀H₉N₃O
• Molecular Weight: 187.198
• Mol File: 28735-28-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 359.5°C at 760 mmHg
• Flash Point: 131.2°C
• Density: 1.181g/cm³
• Vapor Pressure: 4.9E-05mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: 3-methoxy-5-phenyl-1,2,4-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methoxy-5-phenyl-1,2,4-triazine(28735-28-6)
• EPA Substance Registry System: 3-methoxy-5-phenyl-1,2,4-triazine(28735-28-6)

Safety Data

• Hazardous Substances Data: 28735-28-6(Hazardous Substances Data)

Upstream product

• 124-41-4 sodium methylate 
• 28735-27-5 3-methylthio-5-phenyl-1,2,4-triazine 
• 6908-73-2 (E)-1-styrylpyrrolidine 
• 192210-63-2 3-methylthio-6-methoxy-1,2,4,5-tetrazine 
• 122-78-1 phenylacetaldehyde 
• 81930-31-6 3,6-bis(methoxy)-1,2,4,5-tetrazine 

Downstream Products

• 31952-61-1 5-phenyl-1,2,4-triazin-3(2H)-one 
• 942-60-9 5-phenyl-1,2,4-triazin-3-amine 
• 31947-28-1 2-methyl-5-phenyl-1,2,4-triazin-3(2H)-one 
• 49597-47-9 3-methoxy-5-phenyl-2,5-dihydro-1,2,4-triazine 
• 74930-69-1 2-ethyl-5-phenyl-1,2,4-triazin-3(2H)-one 
• 74930-68-0 2-ethyl-3-methoxy-5-phenyl-2,5-dihydro-1,2,4-triazine 
• 28735-29-7 3-hydrazino-5-phenyl-[1,2,4]triazine 

Relevant articles and documents

Selective N1/N4 1,4-Cycloaddition of 1,2,4,5-Tetrazines Enabled by Solvent Hydrogen Bonding

An unprecedented 1,4-cycloaddition (vs 3,6-cycloaddition) of 1,2,4,5-tetrazines is described with preformed or in situ generated aryl-conjugated enamines promoted by the solvent hydrogen bonding of hexafluoroisopropanol (HFIP) that is conducted under mild reaction conditions (0.1 M HFIP, 25 °C, 12 h). The reaction constitutes a formal [4 + 2] cycloaddition across the two nitrogen atoms (N1/N4) of the 1,2,4,5-tetrazine followed by a formal retro [4 + 2] cycloaddition loss of a nitrile and aromatization to generate a 1,2,4-triazine derivative. The factors that impact the remarkable change in the reaction mode, optimization of reaction parameters, the scope and simplification of its implementation through in situ enamine generation from aldehydes and ketones, the reaction scope for 3,6-bis(thiomethyl)-1,2,4,5-tetrazine, a survey of participating 1,2,4,5-tetrazines, and key mechanistic insights into this reaction are detailed. Given its simplicity and breath, the study establishes a novel method for the simple and efficient one-step synthesis of 1,2,4-triazines under mild conditions from readily accessible starting materials. Whereas alternative protic solvents (e.g., MeOH vs HFIP) provide products of the conventional 3,6-cycoladdition, the enhanced hydrogen bonding capability of HFIP uniquely results in promotion of the unprecedented formal 1,4-cycloaddition. As such, the studies represent an example of not just an enhancement in the rate or efficiency of a heterocyclic azadiene cycloaddition by hydrogen bonding catalysis but also the first to alter the mode (N1/N4 vs C3/C6) of cycloaddition.

Pharmacologically active substituted 1,2,4-triazines

Substituted 1,2,4-triazines, compositions thereof and methods of using same are described. The compounds of the invention exhibit a wide range of pharmacological activity including anti-inflammatory, analgesic, anti-pyretic, hypotensive and central nervous system effects.