30362-01-7

Basic information

• Product Name: 2,4,6-tris(dibromomethyl)-1,3,5-triazine
• Synonyms: 1,3,5-triazine, 2,4,6-tris(dibromomethyl)-; 2,4,6-Tris(dibromomethyl)-1,3,5-triazine; 2,4,6-TRIS(DIBROMOMETHYL)-S-TRIAZINE
• CAS NO: 30362-01-7
• Molecular Formula: C₆H₃Br₆N₃
• Molecular Weight: 596.5321
• Mol File: 30362-01-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 475.3°C at 760 mmHg
• Flash Point: 241.2°C
• Density: 2.992g/cm³
• Vapor Pressure: 9.67E-09mmHg at 25°C
• Refractive Index: 1.755
• CAS DataBase Reference: 2,4,6-tris(dibromomethyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(dibromomethyl)-1,3,5-triazine(30362-01-7)
• EPA Substance Registry System: 2,4,6-tris(dibromomethyl)-1,3,5-triazine(30362-01-7)

Safety Data

• Hazardous Substances Data: 30362-01-7(Hazardous Substances Data)

Upstream product

• 823-94-9 2,4,6-trimethyl-s-triazine 
• 75-05-8 acetonitrile 
• 3252-43-5 dibromoacetonitrile 

Relevant articles and documents

Nitrogenous macrocyclic compounds

PCT No. PCT/US96/04215 Sec. 371 Date Sep. 19, 1997 Sec. 102(e) Date Sep. 19, 1997 PCT Filed Mar. 27, 1996 PCT Pub. No. WO96/30377 PCT Pub. Date Oct. 3, 1996Novel macrocyclic compounds are constructed to include large cyclic structures that are interrupted by at least one ring system. Each interrupting ring system includes two bridgehead atoms. Bridgehead atoms are bonded to one or more bridges that interconnect one or more ring systems thereby forming a large cyclic structure. Located in each bridge are two or more nitrogenous moieties that are derivatized with chemical functional groups. The ring systems can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring. These can also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the macrocyclic compounds. In accordance with certain embodiments of the invention, libraries of such macrocyclic compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the library.