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Home Other Building Blocks 2,4,5-Triphenyl-1H-imidazole

2,4,5-Triphenyl-1H-imidazole

CAS No.:
484-47-9
Catalog Number:
AG003FM9
Molecular Formula:
C21H16N2
Molecular Weight:
296.3651
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
97%
In Stock USA
United States
$55
- +
25g
97%
In Stock USA
United States
$125
- +
Product Description
Catalog Number:
AG003FM9
Chemical Name:
2,4,5-Triphenyl-1H-imidazole
CAS Number:
484-47-9
Molecular Formula:
C21H16N2
Molecular Weight:
296.3651
MDL Number:
MFCD00005187
IUPAC Name:
2,4,5-triphenyl-1H-imidazole
InChI:
InChI=1S/C21H16N2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H,(H,22,23)
InChI Key:
RNIPJYFZGXJSDD-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)c1nc(c([nH]1)c1ccccc1)c1ccccc1
EC Number:
207-606-6
UNII:
Q6K46G80ZD
Properties
Complexity:
351  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
296.131g/mol
Formal Charge:
0
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
296.373g/mol
Monoisotopic Mass:
296.131g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
28.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5  
Literature
Title Journal
A peroxide-bridged imidazole dimer formed from a photochromic naphthalene-bridged imidazole dimer. Physical chemistry chemical physics : PCCP 20120428
4-[4,5-Bis(pyridin-2-yl)-1H-imidazol-2-yl]phenol monohydrate. Acta crystallographica. Section E, Structure reports online 20110101
Activation parameters for the recombination reaction of intramolecular radical pairs generated from the radical diffusion-inhibited HABI derivative. The journal of physical chemistry. A 20080710
Antinociceptive and antiinflammatory activities and QSAR studies on 2-substituted-4,5-diphenyl-1H-imidazoles. Bioorganic & medicinal chemistry 20070115
Singlet oxygen generation from lophine hydroperoxides. Luminescence : the journal of biological and chemical luminescence 20070101
Organic nanocrystals with tunable morphologies and optical properties prepared through a sonication technique. Physical chemistry chemical physics : PCCP 20060728
Simulation of the pressure-driven wurtzite to rock salt phase transition in nanocrystals. Physical chemistry chemical physics : PCCP 20060728
Lophine derivatives as versatile analytical tools. Biomedical chromatography : BMC 20030101
Synthesis of fluorescent diarylethenes having a 2,4,5-triphenylimidazole chromophore. The Journal of organic chemistry 20010810
Properties