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Home Other Building Blocks 2,4,6-Triphenyl-1,3,5-triazine

2,4,6-Triphenyl-1,3,5-triazine

CAS No.:
493-77-6
Catalog Number:
AG003FO3
Molecular Formula:
C21H15N3
Molecular Weight:
309.3639
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$74
- +
25g
95%
In Stock USA
United States
$275
- +
Product Description
Catalog Number:
AG003FO3
Chemical Name:
2,4,6-Triphenyl-1,3,5-triazine
CAS Number:
493-77-6
Molecular Formula:
C21H15N3
Molecular Weight:
309.3639
MDL Number:
MFCD00006051
IUPAC Name:
2,4,6-triphenyl-1,3,5-triazine
InChI:
InChI=1S/C21H15N3/c1-4-10-16(11-5-1)19-22-20(17-12-6-2-7-13-17)24-21(23-19)18-14-8-3-9-15-18/h1-15H
InChI Key:
HBQUOLGAXBYZGR-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)c1nc(nc(n1)c1ccccc1)c1ccccc1
EC Number:
207-779-8
UNII:
OI3341XDF6
NSC Number:
46521
Properties
Complexity:
298  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
309.127g/mol
Formal Charge:
0
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
309.372g/mol
Monoisotopic Mass:
309.127g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
38.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5  
Literature
Title Journal
Efficient green thermally activated delayed fluorescence (TADF) from a phenoxazine-triphenyltriazine (PXZ-TRZ) derivative. Chemical communications (Cambridge, England) 20121204
Thermodynamic insights on the structure and energetics of s-triphenyltriazine. The journal of physical chemistry. A 20110825
Chemoselectivity diversity in the reaction of LiNC6F5SiMe3 with nitriles and the synthesis, structure, and reactivity of zirconium mono- and tris[2-(2-pyridyl)tetrafluorobenzimidazolate] complexes. Inorganic chemistry 20101018
Diverse dimerization of molecular tweezers with a 2,4,6-triphenyl-1,3,5-triazine spacer in the solid state. Chemical communications (Cambridge, England) 20100721
An enantiomeric nanoscale architecture obtained from a pseudoenantiomeric aggregate: covalent fixation of helical chirality formed in self-assembled discotic triazine triamides by chiral amplification. Chemistry (Weinheim an der Bergstrasse, Germany) 20060111
Properties