30895-05-7

Basic information

• Product Name: 2,4,6-tris(2-methylpropoxy)-1,3,5-triazine
• Synonyms: 2,4,6-TRIISOBUTOXY-S-TRIAZINE
• CAS NO: 30895-05-7
• Molecular Formula: C₁₅H₂₇N₃O₃
• Molecular Weight: 297.3932
• Mol File: 30895-05-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 393.1°C at 760 mmHg
• Flash Point: 142.7°C
• Density: 1.022g/cm³
• Vapor Pressure: 4.94E-06mmHg at 25°C
• Refractive Index: 1.476
• CAS DataBase Reference: 2,4,6-tris(2-methylpropoxy)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(2-methylpropoxy)-1,3,5-triazine(30895-05-7)
• EPA Substance Registry System: 2,4,6-tris(2-methylpropoxy)-1,3,5-triazine(30895-05-7)

Safety Data

• Hazardous Substances Data: 30895-05-7(Hazardous Substances Data)

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 78-83-1 2-methyl-propan-1-ol 
• 13259-29-5 sodium isobutoxide 

Relevant articles and documents

Antiviral activities of some new 2,4,6-trisubstituted 1,3,5-triazines having alkoxy and/or alkylamino groups

We report the preparation of C3-and CS-symmetrical 2,4,6-trisubstituted 1,3,5-triazine derivatives having alkoxy and/or alkylamino groups and results of biological evaluation of their anti-herpes simplex virus type 1 (anti-HSV-1) activity and cytotoxic activity against Vero cells. New targeted symmetrical molecules were obtained by using a method starting with 2,4,6-trichloro-1,3,5-triazine (1). Among the synthesized compounds, CS-symmetrical tri-aliphatic alkylamino-substituted compound 6s showed high anti-HSV-1 activity (EC50 = 5.4 μM) and low cytotoxicity (CC50 > 200 μM). The results of an SAR study suggested that the presence of two hydrogen bond donor protons of sec-amine functionality in the molecule is an important structural factor for expression of potential anti-HSV-1 activities.